Generic Drug Product Development: Solid Oral Dosage Forms

Contributor(s):

Material type: Text

TextPublication details: New York Marcel Dekker, Inc. 2005Description: 381pISBN:

9780824754600

Subject(s):

Drug Development

DDC classification:

615.19 GEN

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Holdings
Item type	Current library	Item location	Collection	Call number	Status	Date due	Barcode	Item holds
Book	NIMA Knowledge Centre	9th Floor Reading Zone	General	615.19 GEN (Browse shelf(Opens below))	Available		P0005026
Reference Book	NIMA Knowledge Centre	6th Floor Silence Zone	Reference	615.19 GEN (Browse shelf(Opens below))	Not For Loan		P0002287

Total holds: 0

Keeping pace with the latest technologies in the field, this guide describes the development of solid oral generic drug products from project initiation to market approval. Focusing on immediate-release and modified-release dosage forms, the book collects in-depth discussions from more than 30 noted specialists on topics such as quality control, experimental formulation, pharmaceutical ingredients, and bioequivalence, and considers key elements in the formulation of generic drug products including the availability of raw materials, chemical purity. It also highlights constraints in generic drug development that differ from the formulation design of a brand name pharmaceutical product.

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