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Carbamazepin

NDC 0832-6023 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Generic nameCarbamazepine
Labeler / ManufacturerUpsher-Smith Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213311
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsCARBAMAZEPINE (200 mg/1)
Marketing started20210413
Package count1

External sources

Source: openFDA. Public-domain (CC0).