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Bromocriptine Mesylate - 54868-5667-1 - (bromocriptine mesylate)

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Drug Information of Bromocriptine Mesylate

Product NDC: 54868-5667
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: 54868-5667
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076962
Marketing Category: ANDA
Start Marketing Date: 20060908

Package Information of Bromocriptine Mesylate

Package NDC: 54868-5667-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (54868-5667-1)

NDC Information of Bromocriptine Mesylate

NDC Code 54868-5667-1
Proprietary Name Bromocriptine Mesylate
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (54868-5667-1)
Product NDC 54868-5667
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bromocriptine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060908
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


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