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NARATRIPTAN

 
 
Content specific to this active ingredient…

Drug Information
Prescribing and patient information from leading authorities

Drug Master Files
Type 2 master files on file at the FDA

Safety Information
For prescription drugs containing this active ingredient

Exclusivity
Patent and market exclusivity data

Federal Register
FR search results for this API

FDA Approved Labelling
Information found in this drug's package inserts

Research Links
Chemical identification and research citations

Title 21 Code of Federal Regulations
FDA regulations for this API

 
 
 
 
 
 
 
 

 


 

FDA Approval Activities for this Drug…

Amerge (Naratriptan hydrochloride) Tablets, 1 and 2.5 mg Glaxo Wellcome NDA 20-763 Amerge (Naratriptan) Tablets, GlaxoSmithKline NARATRIPTAN HYDROCHLORIDE Tablet; 1MG BASE AMERGE GLAXOSMITHKLINE 020763 NARATRIPTAN HYDROCHLORIDE Tablet; 2.5MG BASE AMERGE GLAXOSMITHKLINE | Naratriptan Tablets, Roxane Laboratories, Inc., Tentative Approval | Naratriptan Tablets, Sandoz Inc., Tentative Approval | Naratriptan (naratriptan hydrochloride)Tablets, Roxane Laboratories, Inc., Approval | Naratriptan (naratriptan hydrochloride) Tablets, Sandoz Inc., Approval | Naratriptan (naratriptan hydrochloride) Tablets, TEVA Pharmaceuticals, Approval | Amerge (naratriptan hydrochloride) Tablets, GlazoSmithKline, Approval | Naratriptan Tablets, Sun Pharmaceutical Industries, Ltd., Approval | Naratriptan Tablets, Indicus Pharma LLC, Approval | Naratriptan Tablets, Apotex Corp., Approval

^ FDA's latest approval appears at the bottom of this list. ^

                                                                   

 

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