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1

The essential guide to generic drugs. Harper & Row, 1986.

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2

Virginia. General Assembly. Joint Commission on Health Care. Therapeutic interchange of chemically dissimilar drugs study pursuant to HJR 734: Report of the Joint Commission on Health Care to the Governor and the General Assembly of Virginia. Commonwealth of Virginia, 2000.

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3

Stauffer, Samuel. Drug comparison handbook. Skidmore-Roth Pub., 1993.

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4

Shargel, Leon, and Isadore Kanfer. Generic drug product development: Specialty dosage forms. Informa Healthcare USA, 2010.

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5

Yong, Chʻŏl-sun. Pi kyŏngguyong cheje ŭi saengmurhakchŏk tongdŭngsŏng hwakpo pangan e taehan yŏnʼgu =: Investigation for establishment of guidelines to assure bioequivalence of nonoral dosage forms. Sikpʻum Ŭiyakpʻum Anjŏnchʻŏng, 2007.

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6

FIP, Bio-International '96 (1996 Tokyo Japan). Bioavailability, bioequivalence and pharmacokinetic studies: FIP Bio-International '96 : International Conference of F.I.P. "Bio-International '96", Tokyo, Japan, April 22-24, 1996. Business Center for Academic Societies Japan, 1996.

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7

Robert, Reilly. Drug comparison handbook. 2nd ed. Skidmore-Roth Pub., 1995.

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8

Drug comparison handbook. 3rd ed. Skidmore-Roth Pub., 1998.

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9

Yu, L. X., and Bing V. Li. FDA bioequivalence standards. AAPS Press/Springer, 2014.

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10

1951-, Jones Byron, ed. Bioequivalence and statistics in clinical pharmacology. Chapman & Hall/CRC, 2006.

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11

Patterson, Scott D. Bioequivalence and statistics in clinical pharmacology. Chapman & Hall/CRC Press, 2005.

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12

Ferm, Max A. How to save dollars with generic drugs: A consumer's guide to high-quality, low-priced medicines. W. Morrow, 1985.

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13

American Society of Health-System Pharmacists., ed. Demystifying opioid conversion calculations: A guide for effective dosing. American Society of Health-System Pharmacists, 2010.

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14

M, Pagliaro Ann, ed. Drug reference guide to brand names and active ingredients. Mosby, 1986.

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15

Kanfer, Isadore. Generic drug product development: International regulatory requirements for bioequivalence. Informa Healthcare, 2010.

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16

Jun, Shao, ed. Statistics in drug research: Methodologies and recent developments. M. Dekker, 2002.

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17

Shargel, Leon. Generic drug product development. CRC, 2007.

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18

Chow, Shein-Chung. Design and analysis of bioavailability and bioequivalence studies. 2nd ed. M. Dekker, 2000.

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19

Chow, Shein-Chung. Design and analysis of bioavailability and bioequivalence studies. 3rd ed. Chapman & Hall/CRC, 2009.

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20

Chow, Shein-Chung. Design and analysis of bioavailability and bioequivalence studies. M. Dekker, 1992.

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21

Copsey, David N., and Sabine Y. J. Delnatte. Genetically Engineered Human Therapeutic Drugs. Macmillan Education UK, 1988. http://dx.doi.org/10.1007/978-1-349-09800-2.

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22

Khatoon, Sayyada. Bark drugs. National Institute of Science Communication and Information Resources, CSIR, 2009.

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23

Khatoon, Sayyada. Bark drugs. National Institute of Science Communication and Information Resources, CSIR, 2009.

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24

Novel therapeutic targets for antiarrhythmic drugs. John Wiley & Sons, 2010.

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25

Hopkins, G. A. Ophthalmic drugs: Diagnostic and therapeutic uses. 5th ed. Butterworth Heinemann/Elsevier, 2007.

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26

Billman, George Edward. Novel therapeutic targets for antiarrhythmic drugs. John Wiley & Sons, 2010.

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27

Bio-International '92 (2nd 1992 Bad Homburg, Germany). Bio-international: Bioavailability, bioequivalence and pharmacokinetics. Medpharm, 1993.

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28

Morganroth, Joel, and E. Neil Moore, eds. Cardiac Arrhythmias: New Therapeutic Drugs and Devices. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4613-2595-6.

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29

Davis, Peter. Managing medicines: Public policy and therapeutic drugs. Open University Press, 1997.

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30

Maddison, Jill E. Therapeutic update. 2nd ed. University of Sydney Post Graduate Foundation in Veterinary Science, 1996.

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31

Maddison, Jill E. Therapeutic update. University of Sydney. Post Graduate Committee in Veterinary Science, 1994.

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32

European Drug Directory. Intercept Ltd, 1992.

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33

European drug directory =: Dictionnaire européen des médicaments et leurs équivalents. 2nd ed. Semp, 1992.

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34

(Editor), Isadore Kanfer, and Leon Shargel (Editor), eds. Generic Drug Product Development: Bioequivalence Issues (Drugs and the Pharmaceutical Sciences). Informa Healthcare, 2007.

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35

Niazi, Sarfaraz K. Handbook of Bioequivalence Testing (Drugs and the Pharmaceutical Sciences). Informa Healthcare, 2007.

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36

Pigeot, Iris, Dieter Hauschke, and Volker Steinijans. Bioequivalence Studies in Drug Development: Methods and Applications (Statistics in Practice). Wiley, 2007.

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37

J, Jackson André, ed. Generics and bioequivalence. CRC, 1994.

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38

G, Welling Peter, Tse Francis L. S, and Dighe Shrikant V, eds. Pharmaceutical bioequivalence. Dekker, 1991.

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39

Conduct and analysis of bioavailability and bioequivalence studies. Health Canada, 1996.

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40

Mosby's Genrx1999: The Complete Reference for Generic and Brand Drugs. 9th ed. C.V. Mosby, 1999.

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41

Mosby's genRx: The complete reference for generic and brand drugs. 9th ed. Mosby, 1999.

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42

Mosby's Drug Consult 2006 (Mosby's Drug Consult). Mosby, 2005.

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43

Mosby's Genrx 1999: The Complete Reference for Generic and Brand Drugs (9th ed). 9th ed. Mosby-Year Book, 1998.

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44

Turning molecules into medicines for the public health. National Cancer Institute, National Institutes of Health, 2000.

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45

Mosby's GenRx: A comprehensive reference for generic and brand prescription drugs. Mosby, 2001.

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46

2001 Mosby's GenRx: Comprehensive Reference for Generic & Brand Prescription... C.V. Mosby, 2000.

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47

Genrx. 2001 Mosby's GenRx: The Complete Reference for Generic and Brand Drugs (CD-ROM for Windows and Macintosh). C.V. Mosby, 2000.

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48

Book, Mosby-Year. Mosby's Genrx 2000: A Comprehensive Reference for Generic and Brand Drugs (Mosby's Genrx, 2000). C.V. Mosby, 2000.

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49

P, Shah Vinod, and Maibach Howard I, eds. Topical drug bioavailability, bioequivalence, and penetration. Plenum Press, 1993.

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50

Design and Analysis of Bioavailability and Bioequivalence Studies, Third Edition (Chapman & Hall/Crc Biostatistics Series). 3rd ed. Chapman & Hall/CRC, 2008.

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