FDA NDC Directory · JSON-LD · Markdown

Carbamazepine

NDC 51672-4005 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074649
Dosage form / routeTABLET · ORAL
Active ingredientsCARBAMAZEPINE (200 mg/1)
Marketing started19961003
Package count3

External sources

Source: openFDA. Public-domain (CC0).