Generic drug product development
bioequivalence issues
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Author
Contributions
- Kanfer, Isadore. - Contributor
- Shargel, Leon, 1941- - Contributor
Publication
2008 - Informa Healthcare, New York, New York (State)
Language
English
Word Count
66,000 words, Guess
Page Count
264 pages
Identifiers
- ISBN-100849377846
- ISBN-139780849377846
- LibraryThing8416123
- Goodreads1449447
- Library of Congress Control Number2007039078
and 2 more
- OCLC Control Number173469782
- Open LibraryOL18499982M
Classifications
- DDC615/.1
- LCCRM301.45 .G42 2008
- DDC615.19
Subjects
Topics
DrugsMethodsMedicalTestingTabletsStandardsPharmacologyDosage formsGeneric drugsDrugs, dosageDrug ApprovalDrugs, GenericDrug developmentBiopharmaceuticsMedical / NursingSolid dosage formsLaw and legislationMedical / PharmacologyBiological AvailabilityTherapeutic EquivalencyPharmaceutical industryTherapeutic equivalencyDrugs -- BioavailabilityPharmaceutical ChemistryPharmaceutical technologyDrugs, generic substitutionDrugs -- Therapeutic equivalency
Series Statement
- Drugs and the pharmaceutical sciences -- 180
Links
Other Editions
- Generic drug product development: bioequivalence issues
Show 5 more editions
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