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Journal articles on the topic 'Indian Pharmacopoeia'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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1

Avtina, N. V., A. V. Prasolova, E. T. Zhilyakova, and T. N. Glizhova. "Comparative analysis of Russian and international requirements for soft dosage forms." Farmaciya (Pharmacy) 73, no. 3 (2024): 24–29. http://dx.doi.org/10.29296/25419218-2024-04-05.

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Introduction. In the Russian Federation, the latest version of the State Pharmacopoeia, XV edition, has been developed and is actively used. (entered into force on September 1, 2023). However, when developing and introducing various medicines into production, pharmaceutical services are forced to turn to GMP and GLP standards to bring the requirements into compliance with European standards. In this connection, it is relevant to conduct a comparative analysis of the regulatory requirements imposed, in particular, on soft dosage forms, in order to identify their similarities and differences. Th

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Singh, K. K., Rajeev Singh Raghuvanshi, and Mohammad Asif. "The exploring role and responsibility of Indian pharmacopoeia commission: An introduction." Journal of Education Technology in Health Sciences 10, no. 3 (2024): 64–68. http://dx.doi.org/10.18231/j.jeths.2023.015.

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: This article emphasise on the Journey of Indian Pharmacopoeia and its parent organisation, the Indian Pharmacopoeia Commission (IPC) as setting up standards for maintaining the efficacy and quality of drugs used for the treatment of diseases prevailing in India. This study attempts to explore Indian Pharmacopoeial growth and general awareness among the scientists, research scholars, drug manufacturers, testing laboratories, healthcare professionals and other stakeholders for their compliance and usage. This article describe the functions of IP Commission such as revision and publication of t

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Kovaleva, E. L., O. A. Matveeva, V. V. Shelestova, and K. A. Balatskaya. "Pharmacopoeias’ and manufacturers’ requirements for the quality of hard gelatin capsule shells." Regulatory Research and Medicine Evaluation 14, no. 6 (2024): 620–33. https://doi.org/10.30895/1991-2919-2024-14-6-620-633.

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INTRODUCTION. The lack of national requirements regulating the quality of empty hard gelatin capsule shells (before filling with medicines) causes difficulties not only for capsule developers and manufacturers but also for experts evaluating regulatory submissions. This necessitates a comparative analysis of Russian and international requirements for the quality of hard gelatin capsule shells in order to draft a pharmacopoeia monograph on empty hard gelatin capsule shells.AIM. This study aimed to analyse the level of quality requirements for hard gelatin capsule shells, the selection of qualit

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Munirathnam, Jayaprakash, and Gowri Radhakrishnan. "Comparison of Monographs of Indian Pharmacopeia with BP and USP Pharmacopeia’s." International Journal of Drug Regulatory Affairs 11, no. 1 (2023): 6–14. http://dx.doi.org/10.22270/ijdra.v11i1.572.

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The objective of this study is to emphasis on the importance of the chromatographic testing methods updates to evaluate the quality of drug products and drug substances. Indian pharmacopeial monographs compared with United States pharmacopeia and British pharmacopoeia monographs for the critical testing parameters. The monographs of most commonly prescribed or sold Tablets like Paracetamol, Amoxycillin, Co-amoxiclav, Losartan potassium and its drug substances were selected for this comparative study. The comparison was made to the critical tests like assay and related substances for drug subst

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Vivekanandan, Kalaiselvan, Hemant Sharma, and Gyanendra Nath Singh. "Quality Standards for Antiretrovirals in Indian Pharmacopoeia." Drug Information Journal 46, no. 5 (2012): 581–86. http://dx.doi.org/10.1177/0092861512450568.

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6

Kumar, KN Sunil. "Herbal Pharmacopoeias– an overview of international and Indian representation." Journal of Ayurvedic and Herbal Medicine 1, no. 3 (2015): 59–60. http://dx.doi.org/10.31254/jahm.2015.1301.

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Pharmacopoeia, literally means “drug-making”, technically is a book published by the authority of a government or a medical or pharmaceutical society containing directions for the identification of medicines, shortly a legal document containing standards for medicinal commodities. The word is derived from Ancient Greek word pharmakopoiia having three words in it - pharmakon meaning ‘a drug’, the verb-stem poi meaning 'make' and abstract noun ending ia; cumulatively meaning 'drug-mak-ing'. The Greek spellings φ (f), κ (k) and οι (oi) are respectively written as ph, c, and oe in early modern edi

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Berra, Jorge Luis, Silvia Chernigoy, Karina Alvarez, and Maria Jose Wernisch. "Ashwagandha under fire: A critical scientific analysis of regulatory decisions." International Journal of Ayurveda Research 5, no. 3 (2024): 148–53. http://dx.doi.org/10.4103/ijar.ijar_192_24.

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Ashwagandha (Withania somnifera [L.] Dunal) is one of the most renowned Ayurvedic medicinal plants, extensively used in traditional Indian medicine systems such as Ayurveda, Siddha, Unani, and Sowa Rigpa for millennia. Its medicinal uses of the root are documented in ancient texts such as the Charaka samhita, Sushruta samhita, and various Nighantus. Recognized globally, Ashwagandha is included in numerous pharmacopoeias, including the Ayurvedic Pharmacopoeia of India (API), British Pharmacopoeia, and United States Pharmacopoeia. Despite its extensive use and documented benefits, Ashwagandha fa

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MURALI R, PRAVEENA B, and BALAMURUGAN K. "Invitro evaluation of generic vs branded product of metformin tablet." World Journal of Advanced Research and Reviews 21, no. 3 (2024): 1490–95. http://dx.doi.org/10.30574/wjarr.2024.21.3.0768.

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The main aim and objective of present research work is to evaluate and compare the standards concerning quality of generic and branded anti hyperglycemic drug (Metformin Hcl). Metformin tablets are evaluated as per standard protocol and results shows that branded and generic meets the pharmacopoeial specifications. All tablets passed the test of weight variation, hardness, thickeness, friability, disintegration, dissolution and assay as per Indian pharmacopoeia. Both the generic and branded tablets of metformin shows similar results. So, health care professionals are suggested to prescribe gen

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MURALI, R., B. PRAVEENA, and K. BALAMURUGAN. "Invitro evaluation of generic vs branded product of metformin tablet." World Journal of Advanced Research and Reviews 21, no. 3 (2024): 1490–95. https://doi.org/10.5281/zenodo.14135710.

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The main aim and objective of present research work is to evaluate and compare the standards concerning quality of generic and branded anti hyperglycemic drug (Metformin Hcl). Metformin tablets are evaluated as per standard protocol and results shows that branded and generic meets the pharmacopoeial specifications. All tablets passed the test of weight variation, hardness, thickeness, friability, disintegration, dissolution and assay as per Indian pharmacopoeia. Both the generic and branded tablets of metformin shows similar results. So, health care professionals are suggested to prescribe gen

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10

Kalra, Sanjay, Siddharth Shah, Subhankar Chowdhury, and AK Das. "Indian Public Health Standards 2012 and the diabetes pharmacopoeia." Indian Journal of Endocrinology and Metabolism 17, no. 7 (2013): 1. http://dx.doi.org/10.4103/2230-8210.119485.

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Nair, Gopakumar G. "A CLARION CALL TO ALL INDIANS TO FACILITATE INTENSE RESEARCH ON NATURAL PRODUCTS." INDIAN DRUGS 57, no. 01 (2020): 5–6. http://dx.doi.org/10.53879/id.57.01.p0005.

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More than 100 years before India was recognised as the “Generic Capital” or “Pharmacy of the World, India was acclaimed for the “Materia Medica” and the extensive research on natural products by Sir Col. Dr. Ram Nath Chopra, the father of Indian Pharmacology. In fact, Dr. M.L. Shroff got inspired from Sir R.N. Chopra and started the first Pharmacy course at Banaras Hindu University in 1932. Every student (even veterans) of Pharmacy should know that Drugs Act, 1940 (later renamed as Drugs and Cosmetics Act) as well as formal courses in Ayurveda, Siddha and Unani were started under his mentorshi

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Tyagi, Sunil. "Use of Electronic Information Resources at the Indian Pharmacopoeia Commission." DESIDOC Journal of Library & Information Technology 32, no. 2 (2012): 171–78. http://dx.doi.org/10.14429/djlit.32.2.1604.

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13

Prakash, Jai, Sushma Srivastava, R. S. Ray, Neha Singh, Roshni Rajpali, and Gyanendra Nath Singh. "Current Status of Herbal Drug Standards in the Indian Pharmacopoeia." Phytotherapy Research 31, no. 12 (2017): 1817–23. http://dx.doi.org/10.1002/ptr.5933.

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14

Raman, Ramya, and Anantanarayanan Raman. "Medical Stores in 1865, Pharmacist Training and Pharmacopoeias in India Until the Launch of the Indian Pharmacopoeia in 1955." Current Science 114, no. 06 (2018): 1358. http://dx.doi.org/10.18520/cs/v114/i06/1358-1366.

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15

Sunte, Bramhadev Tukaram, Aditya Navnath Shinde, and Vaibhav Ravindra Vaidya. "Screening of Marketed Formulations of Shatavari Tablets to Establish Pharmaceutical Equivalence." Journal of Drug Delivery and Therapeutics 13, no. 8 (2023): 56–59. http://dx.doi.org/10.22270/jddt.v13i8.6173.

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Using an in vitro dissolving research, compare the pharmacological equivalent of three brands of Shatavari tablets sold in India. According to IP rules, the dissolution was performed using apparatus I (the paddle device). According to the Indian Pharmacopoeia, evaluation of physicochemical characteristics including weight variation test, content uniformity test, hardness test, friability test, disintegration test, and dissolution test was conducted. For weight fluctuation, content homogeneity, hardness, friability, disintegration time, and dissolving study, all brands complied with official sp

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Rastogi, Shruti, M. Kalaivani, Amandeep K. Bhatia, Jai Prakash, and G. N. Singh. "Implementing the Principle of the 3 Rs Through the Indian Pharmacopoeia." Therapeutic Innovation & Regulatory Science 49, no. 5 (2015): 750–55. http://dx.doi.org/10.1177/2168479015572371.

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17

SANTOSH, K. TALWAR, K. RASTOGI V., and C. SAXENA R. "Spectral Studies of some New Biologically Active Compounds." Journal of Indian Chemical Society Vol. 68, Jul 1991 (1991): 402–3. https://doi.org/10.5281/zenodo.6157748.

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Central Indian Pharmacopoeia Laboratory, Ghaziabad-201 002 Department of Physics, Lajpat Rai College, Sahibabad-201 005 Department of Chemistry, M. M. College, Modi Nagar-201 204 <em>Manuscript received 22 February 1990, revised 10 July 1991, accepted 17 July 1991</em> Spectral Studies of some New Biologically Active Compounds.

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Anjali, Pawar* Shreya Sabale Deven Pardeshi Sneha Vikhe. "A Comparative Analysis of In-Process Quality Control Parameters of Pantoprazole Gastro-Resistant Tablets." International Journal of Pharmaceutical Sciences 3, no. 5 (2025): 1364–75. https://doi.org/10.5281/zenodo.15378649.

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Objectives: This study aimed to evaluate and compare the quality control standards of four different brands of pantoprazole gastro-resistant tablets IP 20 mg, which are commonly prescribed by medical practitioners in the surrounding area. Method: Four brands, labelled A, B, C, and D, were assessed using various in vitro quality control tests. These tests included physical appearance, thickness measurement, weight variation, hardness, friability, disintegration, and dissolution testing. The dissolution test was performed using the USP Paddle II method, and the drug release was analyzed using a

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Iqbal, P. Mohammed, C. M. Harinarayanan, and Vivek Palengara. "Comparative Pharmacognostic study of market samples of Tagara collected from five different markets of Kerala with the official source plant Valeriana jatamansi Jones ex Roxb." AYU (An International Quarterly Journal of Research in Ayurveda) 44, no. 1 (2023): 17–29. http://dx.doi.org/10.4103/ayu.ayu_361_21.

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Abstract Background: Tagara is a very popular Ayurveda herb used in the treatment insomnia, epilepsy, neurosis, hepatoprotective, anticancerous, and analgesic. Characteristic smell is the typical feature of it. As per the Ayurvedic Pharmacopoeia of India and many other classical texts, rhizomes of Valeriana jatamansi of the family Valerianceae is the accepted source of the drug. From some of the reports from early 1980s, it was found that roots of some aquatic plants such as Nymphoides macrospermum, Nymphoides hydrophylla, Nymphoides indica, and Limnanthemum cristatum were said to be used as T

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Makwana, Sarika, Nikhil Mehere, Swapnil Chaudhary, Prashant Bedarkar, Pro Biswajyoti Patgiri, and C. R. Harisha. "Comparative Pharmacognostical Evaluation of Ashodhita and Gomutra Shodhita Bakuchi (Psoralea corylifolia Linn.) Seed." Asian Pacific Journal of Health Sciences 9, no. 1 (2022): 251–54. http://dx.doi.org/10.21276/apjhs.2022.9.1.57.

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Background: Bakuchi (Psoralea corylifolia Linn.) has immense therapeutic attributes and widely prescribed drug in skin disorders especially Shvitra (vitiligo). Its medicinal usage is found depict in Indian pharmaceutical codex, the Chinese, British and the American pharmacopoeias and in different traditional system of medicines such as Ayurveda, Unani and Siddha. Classic emphasized the Shodhana of Bakuchi seed as pre-treatment before its therapeutic use. Considering this, study was planned for pharmacognostical evaluation of Shodhita and Ashodhita Bakuchi seeds. Materials and Methods: Pharmaco

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Srimukhi Tangellapally, Srimukhi Tangellapally, B. Prashanth B.Prashanth, K. Karthik K.Karthik, Ch Manoj Ch.Manoj, T. Srinivas T.Srinivas, and M. Naresh M.Naresh. "Formulation, Development and Evaluation of ExtendedRelease Tablets of Fenbendazole." International Journal of Pharmaceutical Science Invention 14, no. 3 (2025): 14–28. https://doi.org/10.35629/6718-14031428.

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This study aimed to formulate, develop, and evaluate extended-release tablets of Fenbendazole using various polymers, including Hydroxypropyl Methylcellulose K15 (HPMC K15), Ethyl Cellulose, and Tragacanth. The objective was to enhance the sustained release profile of Fenbendazole while ensuring compliance with the Indian Pharmacopoeia (IP) limits for both pre-compression and post-compression parameters. Different formulations were prepared by the direct compression technique, and their physical characteristics, such as hardness, friability, weight variation, and thickness, were assessed. Addi

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S, Shanmugam, Valarmathi S, and Satheesh Kumars. "STERILITY TESTING PROCEDURE OF OPHTHALMIC OCUSERT ACICLOVIR USED FOR TREATING HERPES SIMPLEX VIRUS." Asian Journal of Pharmaceutical and Clinical Research 10, no. 10 (2017): 344. http://dx.doi.org/10.22159/ajpcr.2017.v10i10.19216.

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Objective: The present work focuses on sterility studies of prepared aciclovir ocusert which is so essential for ophthalmic preparations. According to Indian Pharmacopoeia, the sterility test was performed. Ocuserts are sterile preparations which are placed into cul-de-sac or conjunctival sac. Ophthalmic inserts offer many advantages over conventional dosage forms such as increased ocular residence time, possibility of releasing drugs at a slow and constant rate and accurate dosing. Ocuserts are formulated for treating external ocular diseases such as conjuctivitis, corneal ulcer, and keratoco

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Jadaun, Gaurav Pratap Singh, M. Kalaivani, Mukesh Kumar, Gyanendra Nath Singh, Rajeev Singh Raghuvanshi, and Parveen Jain. "Report of a collaborative study to establish the first Indian Pharmacopoeia reference standard for teriparatide." Biologicals 86 (May 2024): 101755. http://dx.doi.org/10.1016/j.biologicals.2024.101755.

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Parihar, Shweta. "A review on pharmacological activities of Andrographis paniculata." Biological Sciences 02, no. 01 (2022): 155–65. http://dx.doi.org/10.55006/biolsciences.2022.2106.

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Andrographis paniculata, is a very famous herbal plant belonging to the family Acanthaceae that has been used since ancient times. Andrographis paniculata, is also called Kalmegh and ‘King of Bitters'. Andrographis paniculata, has been officially mentioned in Indian Pharmacopoeia It is a chief constituent of many Ayurvedic, Siddha, Unani, formulations which are used in the management of liver-related issues. It is a common herbal medicine used to treat snake and bug bites, diabetes, dysentery, fever, and malaria, abortifacient, cancer lytic, depurative, expectorant, hepatoprotective, hypoglyce

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Parida, S., K. K. Rout, and S. K. Mishra. "METHOD OF IDENTIFICATION AND STANDARDISATION OF VAMSALOCHANA (BAMBOO MANNA)." INDIAN DRUGS 51, no. 01 (2014): 55–58. http://dx.doi.org/10.53879/id.51.01.p0055.

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Present study aims to standardize ‘Vamsalochana’, which is a siliceous concrete material found in the hollow internodes of Bambusa arundinacea (Retz.). It is attributed with varieties of medicinal properties and highly valued in the Indian System of Medicine. Various physicochemical parameters like alcohol soluble extractive, water soluble extractive, total ash, acid insoluble ash were determined according to Ayurvedic Pharmacopoeia of India (API). Microscopic examination revealed the presence of rosette crystals of calcium oxalate. Characteristic colours were obtained when the powder drug tre

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Vivekanandan, Kalaiselvan, Jai Prakash, Kalaivani Muthusamy, and Gyanendra Nath Singh. "Quality Standards and Current Status of Ophthalmic Formulations in Indian Pharmacopoeia and National Formulary of India." Therapeutic Innovation & Regulatory Science 48, no. 3 (2014): 386–92. http://dx.doi.org/10.1177/2168479013513455.

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Poojary, Brinda, Laura Viviani, Alokparna Sengupta, et al. "Future of TABST and LABST in the Indian Pharmacopoeia Monographs A Humane Society International/India Workshop Report." Biologicals 83 (August 2023): 101665. http://dx.doi.org/10.1016/j.biologicals.2023.101665.

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NM Anitha, G Essakky Pandian, and A Kingsly. "Standardization of Anda Neer prepared as per Siddha Literature." World Journal of Advanced Research and Reviews 21, no. 1 (2024): 2640–51. http://dx.doi.org/10.30574/wjarr.2024.21.1.0323.

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Siddha drugs are natural products obtained from herbal, mineral and animal kingdom. Most of the Siddha medicines are effective but they have not been standardized yet. So, there be in a need to progress a standardization technique. Anda Neer is a classical Siddha preparation for curing redness of eye mentioned in the textbook of Siddhar Aruvai Maruthuvam written by Dr. K. S. Uthamarayan.. The aim of this study to estimate quality of Anda Neer by conducting physico-chemical analysis, and other analytical techniques. This study was done based on Pharmacopoeial laboratory for Indian Medicine guid

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NM, Anitha, Essakky Pandian G, and Kingsly A. "Standardization of Anda Neer prepared as per Siddha Literature." World Journal of Advanced Research and Reviews 21, no. 1 (2024): 2640–51. https://doi.org/10.5281/zenodo.13377771.

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Siddha drugs are natural products obtained from herbal, mineral and animal kingdom. Most of the Siddha medicines are effective but they have not been standardized yet. So, there be in a need to progress a standardization technique. Anda Neer is a classical Siddha preparation for curing redness of eye mentioned in the textbook of Siddhar Aruvai Maruthuvam written by Dr. K. S. Uthamarayan.. The aim of this study to estimate quality of Anda Neer by conducting physico-chemical analysis, and other analytical techniques. This study was done based on Pharmacopoeial laboratory for Indian Medicine guid

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Narayana, D. B. Anantha. "PHYTO-PHARMACEUTICAL DEFINITION UNDER DRUG REGULATIONS, INDIA NEEDS AN URGENT REVIEW." INDIAN DRUGS 57, no. 12 (2021): 5–6. http://dx.doi.org/10.53879/id.57.12.p0005.

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Dear Reader, An Amendment to the Drugs and Cosmetics Regulations to permit scientifically developed plant based leads as drugs named “phytopharmaceuticals”, was notified for the first time in November 2015. This regulation has now been further amended and revised to put it under new drug definitions and provided more provisions for greater clarity in 2019. However, having championed these regulations (as part of the Indian Pharmacopoeia Commission’s Expert Committee on Herbals) for nearly a decade a greater number of drugs should have come out through this route given the scientific capability

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Kadu, B. M., S. Bhasme, R. D. Bawankar, and D. R. Mundhada. "Formulation and Evaluation of Rapimelt Tablet of Anti-Vertigo Drug (Lorazepam)." International Journal of PharmTech Research 13, no. 4 (2020): 341–49. http://dx.doi.org/10.20902/ijptr.2019.130405.

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A. Rapimelt tablet of Lorazepam was prepared by direct compression method using Indion 414, Cross Carmellose Sodium and sodium starch glycolate as superdisintegrants with aim to get rapid onset of action, improve bioavailability and to give pleasant taste and better mouth feel. The tablets prepared were evaluated for various parameters like various density parameters, thickness, hardness, friability, disintegration time, wetting time and invitro dissolution time and were found to be within limits as per Indian Pharmacopoeia. FT-IR spectra of physical mixture of Lorazepam with Indion 414showedr

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Pradip, P. Deohate. "Analysis of drug ofloxacin in bulk and single component pharmaceutical tablets by non-aqueous potentiometric titration method." Journal of Indian Chemical Society Vol. 95, May 2018 (2018): 559–62. https://doi.org/10.5281/zenodo.5642942.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India E-mail: pradip222091@yahoo.co.in <em>Manuscript received 05 March 2018, accepted 04 April 2018</em> Analysis of drug ofloxacin in bulk and single component pharmaceutical tablets has been carried out by non-aqueous potentiometric titration method using isopropyl alcohol as the solvent and KOH in isopropyl alcohol as the titrant. The effect of solvent and concentration on potentiometric analysis of drug ofloxacin as well as its analysis in bulk and single component pharmaceutica

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Venkatesh, S., B. N. Babu, K. Latha, R. Alvala, M. B. Reddy, and R. Mullangi. "EVALUATION OF TRAPA BISPINOSA STARCH AS AN ALTERNATIVE TABLET EXCIPIENT TO MAIZE STARCH: ASSESSMENT BY PREFORMULATION AND FORMULATION STUDIES." INDIAN DRUGS 49, no. 08 (2012): 27–32. http://dx.doi.org/10.53879/id.49.08.p0027.

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Starch isolated from Trapa bispinosa (Trapaceae) fruit was studied as an alternative pharmaceutical excipient to maize starch. T. bispinosa starch has been evaluated by series of tests as mentioned in Indian Pharmacopoeia before being used for evaluation. It was tested along with maize starch as an alternative excipient by performing battery of preformulation and formulation tests. Preformulation studies like sieve analysis, micrometry, flow properties, moisture content, swelling index and compatibility studies were done as per recommended procedures. The tablets were prepared by wet and dry g

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Pradip, P. Deohate. "Non-aqueous potentiometric determination of pharmaceutically potent drug diphenhydramine hydrochloride." Journal of Indian Chemical Society Vol. 94, Nov 2017 (2017): 1239–42. https://doi.org/10.5281/zenodo.5636064.

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Department of Chemistry, Shri Radhakisan Laxminarayan Toshniwal College of Science, Akola-444 001, Maharashtra, India <em>E-mail</em> : pradip222091@yahoo.co.in <em>Manuscript received 19 July 2017, revised 06 November 2017, accepted 13 November 2017</em> The non-aqueous potentiometric determination of pharmaceutically potent drug diphenhydramine hydrochloride by performing the titrations using isopropyl alcohol as the solvent and KOH in isopropyl alcohol as the titrant has been carried out. The effect of solvent and concentration on potentiometric determination of this drug has been studied f

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Manimekalai, J., P. Aswini, and K. Nalina Saraswathi. "Standardization and Physicochemical Evaluation of the Drug Raja Elathi Chooranam - A Siddha Polyherbal Formulation." International Journal of Health Sciences and Research 12, no. 5 (2022): 213–27. http://dx.doi.org/10.52403/ijhsr.20220523.

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Siddha drugs are natural products obtained from herbal, herbo-mineral, mineral and animal kingdom. Most of the Siddha medicines are effective but they have not been standardized yet. So, there be in need to progress a standardization technique. Raja Elathi Chooranam is a poly-herbal formulation mentioned in the classical Siddha literature for the medication of Menorrhagia. The aim of this study to estimate quality of Raja Elathi Chooranam by conducting physicochemical analysis, phytochemical analysis and other analytical techniques. This study was done based on Pharmacopoeial laboratory for In

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Tiwari, Ritu, Gaurav Mahalpure, Sharma Rohit, Sakshi Mahalpure, and Tiwari Anuanshika. "A Novel Dissolution Method for Simultaneous Estimation of Sennoside A and Sennoside B in Senna Tablet." Clinical Case Studies and Review Reports 2, no. 1 (2025): 1–14. https://doi.org/10.5281/zenodo.14942872.

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<strong>Abstract</strong> The current method was developed for the small-scale herbal industries established in India or the presented sectors in other countries and for the regulatory interest to amend the Senna tablet monograph stated in Indian Pharmacopoeia. The existing method for the dissolution of Senna tablets was cost-consuming and unsuitable for herbal small-scale industries to assay Senna tablets. The present study indicates a reliable high-performance liquid chromatographic method for quantifying sennoside A and sennoside B in commercial Senna tablets. The separation of sennoside A

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Krishna, K. L., and K. Mruthunjaya. "PHARMACOGNOSTICAL EVALUATION OF JUSTICIA GENDARUSSA BURM." INDIAN DRUGS 49, no. 06 (2012): 18–22. http://dx.doi.org/10.53879/id.49.06.p0018.

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Justicia gendarussa (JG) is a shade-loving, quick-growing, evergreen shrub mostly found in moist areas,which grows along the beds of streams in the Himalayas. In Indian and Chinese traditional medicine,the leaf of the plant is recommended to treat ailments such as fever, hemiplegia, rheumatism, arthritis, headache, earache, muscle pain, respiratory disorders and digestive trouble. The physicochemical and pharmacognostical evaluation was carried out according to the official methods mentioned in The Ayurvedic Pharmacopoeia of India. The parameters such as foreign matter, ash value, moisture con

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Pradhan, Naresh Ch, and Ashish Sarkar. "Therapeutic Potential of Boerhavia diffusa Root Extract in the Management of Eye Diseases: Formulation and Evaluation." Journal of Advances and Scholarly Researches in Allied Education 21, no. 3 (2024): 299–304. https://doi.org/10.29070/zg79b770.

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The therapeutic potential of Boerhavia diffusa (Punarnava) root extract in managing eye diseases is explored in this study. Recognized for its antioxidant, anti-inflammatory, and immunomodulatory properties, Boerhavia diffusa holds promise as a treatment for ocular conditions such as cataracts, diabetic retinopathy, and age-related macular degeneration. The research focuses on the development of a novel Ayurvedic eye drop formulation using aqueous distillate from Boerhavia diffusa roots, complying with Indian Pharmacopoeia standards. Phytochemical analyses, including HPTLC, GC-MS, and HPLC, co

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Husain, Dr Safder, Arish Mohammad Khan Sherwani, and Arish Mohammad Khan Sherwani. "Prevention and Control of Anaemia by Unani Intervention." INTERNATIONAL JOURNAL OF PLANT AND ENVIRONMENT 9, no. 01 (2023): 85–88. http://dx.doi.org/10.18811/ijpen.v9i01.14.

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Anaemia is still common in India, and its prevalence has increased across all age groups. The prevalence of anaemia has increased by 2–9% among infants, pregnant and non-pregnant women, and men, according to data from the National Family Health Survey 5 (NFHS-5)released on November 24, 2021. For over 2000 years, the Unani system of Medicine (USM) a unique and comprehensive medical system, has ruled in terms of theory and practise. Its beliefs and practises differ from western medicine and may not be completely associatedwith it, but they are still significant because they are well-considered,

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Patel, Royal, Anupam Kumar Sachan, Sanjana Chaohan, et al. "Present era of drug safety in India: An overview." Journal of Pharmacovigilance and Drug Research 2, no. 1 (2021): 1–8. http://dx.doi.org/10.53411/jpadr.2021.2.1.1.

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Introduction: Common Adverse Drug Reactions (ADR), evaluated by drug clinical trial studies, whereas an individual or specific population might suffer reactions after prolonged dormancy. Pharmacovigilance (PV) is a scientific investigation dealing with and keeping regular vigil on the drugs being used. Methods: The Indian Pharmacopoeia Commission (IPC) and other regulatory authorities like a National Coordination Committee (NCC) via the Central Drug Standard Control Organization (CDSCO) manage PV activity in synchronicity. Indian Pharmacovigilance (PV) system requires carving, therefore

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Patel, Royal, Anupam Kumar Sachan, Sanjana Chaohan, et al. "Present era of drug safety in India: An overview." Journal of Pharmacovigilance and Drug Research 2, no. 1 (2021): 1–8. https://doi.org/10.5281/zenodo.4904459.

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<strong>Abstract</strong> Common Adverse Drug Reactions (ADR), evaluated by drug clinical trial studies, whereas an individual or specific population might suffer reactions after prolonged dormancy. Pharmacovigilance (PV) is a scientific investigation dealing and keeping regular vigil on the drugs being used. The Indian Pharmacopoeia Commission (IPC) and other regulatory authorities like a National Coordination Committee (NCC) via the Central Drug Standard Control Organization (CDSCO) manage PV activity in synchronicity. Indian Pharmacovigilance (PV) system require carving, therefore the Pharm

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Komal, Patel M. .V. N. .L. Chaitanya* P. Ramalingam G.S. Bharat Y. Padmanabha Reddy Mohammed Gulzar Ahmed. "CURRENT REGULATORY PERSPECTIVE OF HERBAL DRUGS." INDO AMERICAN JOURNAL OF PHARMACEUTICAL SCIENCES o6, no. 05 (2019): 9547–51. https://doi.org/10.5281/zenodo.2783990.

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<em>The current challenging aspect of herbal medicine or traditional system is maintenance of quality, safety and efficacy issues. As there is a global recognition for the herbal drugs as an healing aids, the demand for these traditional system have been increased drastically from 19<sup>th</sup> century to 21<sup>st</sup> century. As the main challenge of this herbal medicine / drugs is maintenance of DNA  finger printing, phytochemical and therapeutic uniformity, lack of Good clinical practices, standard  operating protocols, no proper protocols or guidelines on pharmacokinetic and

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Shazamani, S., Wajeeha Begum, and Syeda Sumaiya. "Therapeutic potential of Murmakki (Commiphora myrrha) in gynaecological disorder: A Unani review." Journal of Drug Delivery and Therapeutics 12, no. 4 (2022): 227–30. http://dx.doi.org/10.22270/jddt.v12i4.5554.

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Murmakki is a well-known and potent herbal drug used in various traditional medicines for its various beneficial effects on different Gynaecological ailments and diseases. It is commonly known as Gum Resin. It Consists of oleogum resin obtained by exudation from the stem of a plant of Commiphora myrrha. It is used in Saudi Arabia, Indian and Western Medicine and is listed in the British pharmacopoeia as an antispasmodic and expectorant. In ancient traditional Persian manuscripts, it has been noted that myrhh acts as a uterine stimulant and probably cause complete abortion. In Unani Medicine, i

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R, NITHYA, Shruthi Deivigarajan, Sindhuja Santhakumar, and Sneha Balakrishnan. "Challenges encountered by health care professionals in monitoring adverse events due to medical devices: A review." Scientific Temper 14, no. 02 (2023): 479–83. http://dx.doi.org/10.58414/scientifictemper.2023.14.2.37.

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Materiovigilance is the term used to characterize any negative outcomes brought on by a medical device. The "Materiovigilance Programme of India" is a plan that has been launched in India to track the unfavorable outcomes of the use of medical devices and to take the necessary action to resolve those unfavorable outcomes. On July 6, 2015, DCGI adopted MvPI at the Indian Pharmacopoeia Commission in Ghaziabad. Factors contributing to underreporting of MDAE are Health care system capacity related, Organizational related barriers, and Industry responsiveness. Challenges faced by healthcare profess

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Aditya, Mane* Anirudha Patil Tejashri Kamble Dr. Nilesh Chougule. "Terbinafine Tablet Quality Control Test Report and Pharmacology: Compliance with Pharmacopeial Standards." International Journal of Pharmaceutical Sciences 2, no. 11 (2024): 548–55. https://doi.org/10.5281/zenodo.14104380.

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This comprehensive report evaluates the quality control and pharmacological profile of Terbinafine tablets, ensuring adherence to Indian Pharmacopoeia (IP) 2022 standards. 1. Identity: Thin Layer Chromatography (TLC) confirmed the presence of Terbinafine. 2. Physical Characteristics: Tablets met IP 2022 specifications for description and disintegration time (≤15 minutes). 3. Chemical Purity: Assay results showed 97.06% of labeled amount. 4. Performance: Dissolution exceeded 75% in 30 minutes. 5.Microbial limits. 6. Assay: 90-110% of labeled amount. Pharmacological Assessment: 1. Mechanism:

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Rajat, Vaishnav, and S. Ranawat Mahendra. "Stability Testing of Ayurvedic Drugs: An Indian Regulatory Perspective." Pharmaceutical and Chemical Journal 9, no. 5 (2022): 1–10. https://doi.org/10.5281/zenodo.13973346.

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he safety and effectiveness of a product are greatly influenced by its stability. Ayurvedic, Siddha, and Unani (ASU) medicine includes single-herb or polyherbal formulations with or without mineral medications and/or drug ingredients derived from animals. Pharmaceutical products have currently undergoing stability testing in accordance with the guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The First Schedule of the Drugs and Cosmetics Act, 1940 includes a concept of shelf l

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Joshi, Suvarna, Sandeepan Mukerjee, Shashikant Vaidya, Gitanjali Talele, Abhay Chowdhary, and Rajesh Shah. "Preparation, standardization and in vitro safety testing of Mycobacterium nosodes (Emtact- polyvalent nosode)." Homeopathy 105, no. 03 (2016): 225–32. http://dx.doi.org/10.1016/j.homp.2016.02.006.

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Background: Most of the nosodes in the homeopathic pharmacopeia have been sourced from obscure pathological material over a century ago; of which no scientific documentation is available. Method: A method for preparation and standardization of univalent and polyvalent Mycobacterium nosodes (labeled as Emtact), using different strains of Mycobacterium tuberculosis was developed. The committee comprising microbiologists, scientist, pharmacist, homeopaths and clinicians had reviewed and approved the method of preparation of nosode. Preparation of the nosode was based on the reference in the Homeo

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Joshi, Devesh Kumar, Krishna Chaitanya Veligandla, Rahul Rathod, and Bhavesh P. Kotak. "In-Vitro Comparative Study of Levocetirizine Dihydrochloride and Montelukast Sodium Release Profiles in Xyzal M Suspension and Other Marketed Syrup Formulations." Journal of Drug Delivery and Therapeutics 13, no. 8 (2023): 32–44. http://dx.doi.org/10.22270/jddt.v13i8.6164.

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Objectives: In-vitro comparative analysis of the release profile of levocetirizine dihydrochloride and montelukast sodium in Xyzal M Suspension and three commercially available syrup formulations. Method: The active components and their impurities were initially assayed in all formulations using a validated HPLC method. The enantiomeric impurities of montelukast sodium in different pH media were determined using the HPLC method specified in the United State Pharmacopoeia (USP) monograph. Additionally, dissolution studies and the soluble fractions of the components were evaluated in pH me

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hubham, Jain S., Agrawal Akhil, and Agrawal Medha. "PHARMACEUTICAL PROCESSING AND STANDARDIZATION OF INDRA VATI." International Ayurvedic Medical Journal 09, no. 3 (2021): 536–43. http://dx.doi.org/10.46607/iamj0409032021.

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Ayurveda is the most ancient system of life, health and cure. It is highly evolved and codified system of life and health science, based on its own unique and original concepts and fundamental principles. Rasa shastra, which starts with a pledge to render a happy, healthy and prosperous life can be considered as an advanced stage of Indian system of medicine. Rasa shastra has large number varieties of Rasaushadhi aiding on Madhumeha (Diabetes Mellitus) but among them ‘Indra Vati’ is one of the significant ones. Though this preparation is not formulated by any pharmacy. CCRAS and DPT. of AYUSH

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Sree, Sravya, and Pasikhanti Shailaja. "Haemovigilance: New approach for safe Blood transfusion." International Journal of Drug Regulatory Affairs 7, no. 4 (2019): 1–7. http://dx.doi.org/10.22270/ijdra.v7i4.352.

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Haemovigilance is an urgent need of the country to identify and prevent occurrence or recurrence of transfusion related adverse reactions, thereby to increase the safety and quality of blood transfusion and blood products administration. Haemovigilance is an organised scheme of monitoring, identifying, reporting, investigating and analysing adverse events and reactions pertinent to transfusion and manufacturing blood products. Thus the information collected will facilitate corrective and preventive actions to minimise the potential risks associated with blood collection, processing and transfu

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