03057nam\a2200385\a\4500 57998 20260819122702.0 260819s2014 flua b 001 0 eng 9781420086355 hbk. : alk. paper 9781420086362 eBook (DNLM)101606012 DNLM/DLC DLC BD-DhIUB 615.19 23 G3261 Generic drug product development : solid oral dosage forms / edited by Leon Shargel, Isadore Kanfer. 2nd ed. Boca Raton, FL : CRC Press/Taylor & Francis Group, c2014. (reprint 2024) xii, 385 p. : ill. ; 25 cm. Drugs and the pharmaceutical sciences ; 129 Includes bibliographical references and index. Active pharmaceutical ingredient / Edward M. Cohen, Steven Sutherland -- Analytical methods development and methods validation for solid oral dosage forms / Quanyin Gao, Dilip R. Sanvordeker -- Experimental formulation development / Isadore Kanfer ... [et al.] -- Scale-up, technology transfer, and process performance qualification / Salah U. Ahmed ... [et al.] -- Drug stability / Pranab K. Bhattacharyya -- Quality control and quality assurance / Loren Gelber -- Drug product performance, in vitro / Pradeep M. Sathe, John Duan, and Lawrence X. Yu -- ANDA regulatory approval process / Timothy W. Ames, Aaron Sigler -- Bioequivalence and drug product assessment, in vivo / Barbara M. Davit, Dale P, Conner -- Statistical considerations for establishing bioequivalence / Charles Bon, Sanford Bolton -- Outsourcing bioavailability and bioequivalence studies to contract research organizations / Patrick K. Noonan -- Post-approval changes and post-marketing surveillance / Lorien Armour, Leon Shargel -- United States Pharmacopeia-National Formulary : its history, organization, and role in harmonization / William Brown, Margareth R.C. Marques -- Legal and legislative hurdles to generic drug development, approval and marketing / Arthur T. Tsien. "This book collects in-depth discussions from more than 30 noted specialists on topics such as quality control, experimental formulations, pharmaceutical ingredients, conventional and modified-release products, and bioequivalence. It considers key elements in the formulation of generic drug products including the availability of raw materials and chemical purity. It contains new chapters on experimental formulation development, and the relationship between the FDA and the United States Pharmacopeia"--Provided by publisher. PHR phr PHAR Omni concept Generic drugs. Solid dosage forms. Drugs, Generic standards. Chemistry, Pharmaceutical standards. Drug Approval. Tablets. Shargel, Leon, 1941- Kanfer, Isadore. ddc BK 57998 58172 0 0 ddc 0 1 IUBL IUBL PHAR 2026-08-13 PURCHASE 5199.00 20174 0 615.19 G3261 030012 2026-08-19 12:30:26 01 10398.00 2026-08-13 BK 0 0 ddc 0 1 IUBL IUBL PHAR 2026-08-13 PURCHASE 5199.00 20174 0 615.19 G3261 030013 2026-08-19 12:30:00 02 10398.00 2026-08-13 BK