FDA NDC Directory · JSON-LD · Markdown

Oxcarbazepine

NDC 72888-088 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameoxcarbazepine
Labeler / ManufacturerAdvagen Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077747
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (300 mg/1)
Marketing started20210319
Package count3

External sources

Source: openFDA. Public-domain (CC0).