Generic drug

Results: 2111



#Item
911Pharmacology / Pharmaceuticals policy / Drugs / Pharmacy / Clinical pharmacology / Generic drug / Medical prescription / Prescription medication / Out-of-pocket expenses / Pharmaceutical sciences / Medicine / Health

Microsoft Word - jj03mar_2012.doc

Add to Reading List

Source URL: www.cga-pdnet.org

Language: English - Date: 2012-04-18 14:54:22
912Pharmaceuticals policy / Pharmacology / Pharmaceutics / Therapeutics / Prescription Drug User Fee Act / Center for Drug Evaluation and Research / Drug Master File / Generic drug / Abbreviated New Drug Application / Food and Drug Administration / Pharmaceutical industry / Pharmaceutical sciences

GDUFA Public Mtg Min[removed]

Add to Reading List

Source URL: www.fda.gov

Language: English
913Pharmaceutical industry / Pharmacy / Clinical pharmacology / Generic drug / Medical prescription / Bioequivalence / Abbreviated New Drug Application / Food and Drug Administration / Pharmaceutical policy / Pharmaceutical sciences / Pharmacology / Pharmaceuticals policy

[removed] c a n a d i a n g e n e r i c p h a r m a c e u t i c a l a s s o c i at i o n Generic manufacturers invest three to six

Add to Reading List

Source URL: www.canadiangenerics.ca

Language: English - Date: 2014-04-24 12:47:38
914Medicine / Health / Pharmaceuticals policy / Pharmacology / Drug safety / New Drug Application / Generic drug / Hospira / Federal Food /  Drug /  and Cosmetic Act / Pharmaceutical sciences / Food and Drug Administration / Pharmaceutical industry

Microsoft Word - 8421889_3

Add to Reading List

Source URL: www.fdalawblog.net

Language: English - Date: 2014-08-19 07:33:23
915Food and Drug Administration / Research / Clinical research / Pharmaceuticals policy / Wyeth v. Levine / Generic drug / Abbreviated New Drug Application / New Drug Application / Approved drug / Pharmaceutical sciences / Pharmaceutical industry / Pharmacology

Generic Drug Manufacturers Post-ANDA Approval Duties With Reference To Labeling Changes: Viability of Federal Preemption Changes: Viability of Federal Preemption Defense Post-Levine

Add to Reading List

Source URL: www.duanemorris.com

Language: English - Date: 2010-05-18 12:47:53
916Pharmacology / Pharmaceutical industry / Pharmaceuticals policy / Wyeth / Wyeth v. Levine / New Drug Application / Federal preemption / Drug Price Competition and Patent Term Restoration Act / Generic drug / Pharmaceutical sciences / Law / Food and Drug Administration

Courts Are Divided on Whether Failure to Warm Claims Against Generic Drug Manufacturers Can Be Preempted

Add to Reading List

Source URL: www.duanemorris.com

Language: English - Date: 2009-03-06 16:49:08
917Pharmacology / Pharmaceutics / Pharmaceuticals policy / Therapeutics / New Drug Application / Drug Master File / Generic drug / Prescription Drug User Fee Act / Form FDA 483 / Pharmaceutical industry / Pharmaceutical sciences / Food and Drug Administration

December 20, 2010: FDA Update regarding Generic Drug User Fees

Add to Reading List

Source URL: www.fda.gov

Language: English
918Pharmaceutical sciences / Pharmacology / Medicare Part D / Medicare / Pharmaceutical industry / Medical prescription / Generic drug / Copayment / Prescription medication / Pharmaceuticals policy / Health / Medicine

Microsoft Word - 0067_Donut_hole_Factsheet.docx

Add to Reading List

Source URL: www.shiip.state.ia.us.

Language: English - Date: 2014-10-27 12:18:14
919User interface techniques / Windows Explorer / Menu bar / Double-click / Submission software / File dialog / Portable Document Format / Dialog box / Computer icon / Software / System software / Computing

eSubmitter Quick Guide - Generic Drug Facility Self-Identification The eSubmitter software enables the electronic submission of regulatory information to FDA. FDA is using eSubmitter to help generic drug companies perfor

Add to Reading List

Source URL: www.fda.gov

Language: English
920Pharmaceuticals policy / Food and Drug Administration / Pharmaceutical industry / Wyeth / Wyeth v. Levine / New Drug Application / Generic drug / Federal Food /  Drug /  and Cosmetic Act / Federal preemption / Pharmaceutical sciences / Pharmacology / Medicine

BOYD[removed]Do Not Delete[removed]:19 PM UNEQUAL PROTECTION UNDER THE LAW: WHY FDA SHOULD USE NEGOTIATED RULEMAKING TO REFORM

Add to Reading List

Source URL: www.cardozolawreview.com

Language: English - Date: 2014-04-22 20:47:55
UPDATE