Bromocriptine mesylate
Bromocriptine Mesylate Tablets, USP
Approved
Approval ID
b89ff149-e33a-46cb-9649-64583e78a7ee
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jul 6, 2017
Manufacturers
FDA
Carilion Materials Management
DUNS: 079239644
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Bromocriptine mesylate
PRODUCT DETAILS
NDC Product Code68151-1305
Application NumberANDA077646
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateSeptember 25, 2015
Generic NameBromocriptine mesylate
INGREDIENTS (7)
BROMOCRIPTINE MESYLATEActive
Quantity: 2.5 mg in 1 1
Code: FFP983J3OD
Classification: ACTIM
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MALEIC ACIDInactive
Code: 91XW058U2C
Classification: IACT
POVIDONE K25Inactive
Code: K0KQV10C35
Classification: IACT
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
ANHYDROUS LACTOSEInactive
Code: 3SY5LH9PMK
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT