FDA NDC Directory · JSON-LD · Markdown

Epitol

NDC 0093-0090 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameCarbamazepine
Labeler / ManufacturerTeva Pharmaceuticals USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070541
Dosage form / routeTABLET · ORAL
Active ingredientsCARBAMAZEPINE (200 mg/1)
Marketing started19900930
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).