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BROMOCRIPTINE

 
 
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…

Bromocriptine Mesylate Capsules USP, 5 mg (base) LEK USA, ANDA 75-100 BROMOCRIPTINE MESYLATE Capsule; 5MG BASE PARLODEL NOVARTIS 074631 BROMOCRIPTINE MESYLATE Tablet; 2.5MG BASE BROMOCRIPTINE MESYLATE LEK 017962 BROMOCRIPTINE MESYLATE Tablet; 2.5MG BASE PARLODEL NOVARTIS | Bromocriptine Mesylate Tablets, Mylan Pharma, Approval | Bromocriptine Mesylate Capsules, Mylan Pharma, Approval | Parlodel (bromocriptine mesylate), Novartis Pharma, Labeling Revision | Bromocriptine Mesylate Capsules, Zydus Pharmaceuticals USA, Inc., Approval | Bromocriptine Mesylate Tablets, Paddock Laboratories, Inc., Approval | Cycloset (bromocriptine mesylate) Tablets, VeroScience, LLC, Approval | Cycloset (bromocriptine mesylate) Tablets, VeroScience, LLC, Labeling Revision | Parlodel, bromocriptine mesylate, Capsule; Oral, Novartis, Labeling Revision | Parlodel, bromocriptine mesylate, Tablet; Oral, Novartis, Labeling Revision

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

                                                                   

 

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