Home > National Drug Code (NDC) > Bromocriptine mesylate

Bromocriptine mesylate - 0781-5325-01 - (Bromocriptine mesylate)

Alphabetical Index


Drug Information of Bromocriptine mesylate

Product NDC: 0781-5325
Proprietary Name: Bromocriptine mesylate
Non Proprietary Name: Bromocriptine mesylate
Active Ingredient(s): 2.5    mg/1 & nbsp;   Bromocriptine mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bromocriptine mesylate

Product NDC: 0781-5325
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074631
Marketing Category: ANDA
Start Marketing Date: 19980113

Package Information of Bromocriptine mesylate

Package NDC: 0781-5325-01
Package Description: 100 TABLET in 1 BOTTLE (0781-5325-01)

NDC Information of Bromocriptine mesylate

NDC Code 0781-5325-01
Proprietary Name Bromocriptine mesylate
Package Description 100 TABLET in 1 BOTTLE (0781-5325-01)
Product NDC 0781-5325
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bromocriptine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19980113
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name BROMOCRIPTINE MESYLATE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Ergolines [Chemical/Ingredient],Ergot Derivative [EPC]

Complete Information of Bromocriptine mesylate


General Information