FDA NDC Directory · JSON-LD · Markdown

Carbamazepine

NDC 51672-4050 · HUMAN PRESCRIPTION DRUG · TABLET, CHEWABLE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075687
Dosage form / routeTABLET, CHEWABLE · ORAL
Active ingredientsCARBAMAZEPINE (200 mg/1)
Marketing started20001024
Package count1

External sources

Source: openFDA. Public-domain (CC0).