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Generic drug
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#	Item
881	Microsoft Word - Mike Russo USPIRG Testimony on Pay-for-Delay Deals Add to Reading List Source URL: uspirg.org Language: English - Date: 2013-07-22 16:37:03 Medicine Pharmaceutical industry Generic drug Public domain Pharmacy Modafinil Copayment Ciprofloxacin Tom DeLay Pharmacology Pharmaceutical sciences Pharmaceuticals policy
882	H. R[removed]One Hundred Tenth Congress of the United States of America AT T H E S E C O N D S E S S I O N Add to Reading List Source URL: www.fda.gov. Language: English Health Food and Drug Administration Food law Pharmacology Pharmaceutical industry Abbreviated New Drug Application Generic drug Federal Food Drug and Cosmetic Act Prescription Drug User Fee Act Pharmaceuticals policy Pharmaceutical sciences Medicine
883	Stability – The Current Status Susan Rosencrance, Ph.D. Deputy Director for Chemistry (Acting) Office of Generic Drugs GPhA/FDA Fall Technical Conference Add to Reading List Source URL: www.fda.gov. Language: English Pharmacology Clinical research Generic drug Public domain Abbreviated New Drug Application Food and Drug Administration Pharmaceutical sciences Pharmaceuticals policy Pharmaceutical industry
884	Revisions to Guidance to Industry 2125fnl.PDF Add to Reading List Source URL: www.fda.gov. Language: English Pharmaceutical sciences Prescription Drug User Fee Act Center for Biologics Evaluation and Research New Drug Application Investigational New Drug FDA Special Protocol Assessment Center for Drug Evaluation and Research Biologic Generic drug Food and Drug Administration Medicine Health
885	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. It was current when produced, but is no longer maintained and may Add to Reading List Source URL: www.fda.gov Language: English Health Pharmaceutical industry Clinical research Food and Drug Administration Generic drug Abbreviated New Drug Application Center for Drug Evaluation and Research Drug Price Competition and Patent Term Restoration Act Kefauver Harris Amendment Pharmaceutical sciences Pharmaceuticals policy Pharmacology
886	The committee will discuss saxagliptin tablets, by Bristol-Myers Squibb, for the treatment of hyperglycemia in adults with type 2 diabetes mellitus Add to Reading List Source URL: www.fda.gov Language: English Clinical research Clinical pharmacology Pharmaceuticals policy Generic drug Abbreviated New Drug Application Food and Drug Administration Bioequivalence New Drug Application Drug discovery Pharmaceutical sciences Pharmacology Pharmaceutical industry
887	U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only. This content has not been altered or updated since it was archived Add to Reading List Source URL: www.fda.gov Language: English Research Clinical research Pharmaceutical industry Bioequivalence Pharmacokinetics Generic drug Center for Drug Evaluation and Research Pharmaceutical sciences Pharmacology Food and Drug Administration
888	Providing key policy setters and decision makers in the global health sector with unique and transformational insights into healthcare dynamics derived from granular analysis of information. IMPACT OF PATENT SETTLEMENTS Add to Reading List Source URL: www.gphaonline.org Language: English - Date: 2013-07-09 11:42:00 Pharmaceuticals policy Pharmaceutical industry Pharmacy Generic drug Drug Price Competition and Patent Term Restoration Act Novartis Patent Adderall Pfizer Pharmaceutical sciences Pharmacology Health
889	Complex Generic Drugs Robert Lionberger, Ph.D. Deputy Director for Science (acting) Office of Generic Drugs Center for Drug Evaluation and Research, FDA The views presented are those of the authors and do not necessarily Add to Reading List Source URL: www.fda.gov Language: English Pharmacology Pharmaceuticals policy Food and Drug Administration Abbreviated New Drug Application Generic drug Regulatory science Center for Drug Evaluation and Research Drug development Pharmaceutical sciences Pharmaceutical industry Clinical research
890	Lifesaving Drugs at Lower Costs Introduction The Food and Drug Administration (FDA) began approving generic (unbranded) prescription drugs around 30 years ago, and generic drugs are now saving consumers more than one tri Add to Reading List Source URL: www.theamericanconsumer.org Language: English - Date: 2014-10-17 12:07:50 Pharmaceuticals policy Biosimilar Biotechnology Drugs Pharmaceutical industry Biologic Food and Drug Administration Hospira Generic drug Pharmaceutical sciences Pharmacology Clinical research

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