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Bromocriptine mesylate - 0574-0106-01 - (Bromocriptine mesylate)

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Drug Information of Bromocriptine mesylate

Product NDC: 0574-0106
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: 0574-0106
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077646
Marketing Category: ANDA
Start Marketing Date: 20081001

Package Information of Bromocriptine mesylate

Package NDC: 0574-0106-01
Package Description: 24 BOTTLE in 1 CARTON (0574-0106-01) > 100 TABLET in 1 BOTTLE

NDC Information of Bromocriptine mesylate

NDC Code 0574-0106-01
Proprietary Name Bromocriptine mesylate
Package Description 24 BOTTLE in 1 CARTON (0574-0106-01) > 100 TABLET in 1 BOTTLE
Product NDC 0574-0106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bromocriptine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081001
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, 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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