Carbidopa Tablets, 25 mg
Carbidopa Tablets, 25 mg
Approved
Approval ID
97e7696c-5220-e5c3-9429-7fad5eda33fe
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 14, 2023
Manufacturers
FDA
Alvogen Inc.
DUNS: 008057330
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Carbidopa Tablets, 25 mg
PRODUCT DETAILS
NDC Product Code47781-332
Application NumberANDA204291
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateApril 17, 2012
Generic NameCarbidopa Tablets, 25 mg
INGREDIENTS (5)
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CARBIDOPAActive
Quantity: 25 mg in 1 1
Code: MNX7R8C5VO
Classification: ACTIM
FD&C YELLOW NO. 6Inactive
Code: H77VEI93A8
Classification: IACT
MICROCRYSTALLINE CELLULOSEInactive
Code: OP1R32D61U
Classification: IACT