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Carbamazepine

NDC 62332-421 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219939
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsCARBAMAZEPINE (200 mg/1)
Marketing started20250726
Package count2

External sources

Source: openFDA. Public-domain (CC0).