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Bromocriptine Mesylate - 0781-2119-01 - (bromocriptine mesylate)

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Drug Information of Bromocriptine Mesylate

Product NDC: 0781-2119
Proprietary Name: Bromocriptine Mesylate
Non Proprietary Name: bromocriptine mesylate
Active Ingredient(s): 5    mg/1 & nbsp;   bromocriptine mesylate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Bromocriptine Mesylate

Product NDC: 0781-2119
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017962
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19780628

Package Information of Bromocriptine Mesylate

Package NDC: 0781-2119-01
Package Description: 100 CAPSULE in 1 PACKAGE (0781-2119-01)

NDC Information of Bromocriptine Mesylate

NDC Code 0781-2119-01
Proprietary Name Bromocriptine Mesylate
Package Description 100 CAPSULE in 1 PACKAGE (0781-2119-01)
Product NDC 0781-2119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bromocriptine mesylate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19780628
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Sandoz Inc
Substance Name BROMOCRIPTINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Ergolines [Chemical/Ingredient],Ergot Derivative [EPC]

Complete Information of Bromocriptine Mesylate


General Information