VIGABATRIN
VIGABATRIN
Approved
Approval ID
663f447f-7b22-4e3e-942a-2df7713aa028
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 10, 2022
Manufacturers
FDA
Biocon Pharma Inc.
DUNS: 080000063
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
VIGABATRIN
PRODUCT DETAILS
NDC Product Code70377-089
Application NumberANDA213390
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateNovember 10, 2022
Generic NameVIGABATRIN
INGREDIENTS (2)
VigabatrinActive
Quantity: 500 mg in 10 mL
Code: GR120KRT6K
Classification: ACTIB
PovidoneInactive
Code: FZ989GH94E
Classification: IACT