CYCLOSET - 68012-258-60 - (bromocriptine mesylate)

Alphabetical Index


Drug Information of CYCLOSET

Product NDC: 68012-258
Proprietary Name: CYCLOSET
Non Proprietary Name: bromocriptine mesylate
Active Ingredient(s): .8    mg/1 & nbsp;   bromocriptine mesylate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CYCLOSET

Product NDC: 68012-258
Labeler Name: Santarus, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020866
Marketing Category: NDA
Start Marketing Date: 20101115

Package Information of CYCLOSET

Package NDC: 68012-258-60
Package Description: 600 TABLET in 1 BOTTLE (68012-258-60)

NDC Information of CYCLOSET

NDC Code 68012-258-60
Proprietary Name CYCLOSET
Package Description 600 TABLET in 1 BOTTLE (68012-258-60)
Product NDC 68012-258
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bromocriptine mesylate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101115
Marketing Category Name NDA
Labeler Name Santarus, Inc.
Substance Name BROMOCRIPTINE MESYLATE
Strength Number .8
Strength Unit mg/1
Pharmaceutical Classes Ergolines [Chemical/Ingredient],Ergot Derivative [EPC]

Complete Information of CYCLOSET


General Information