FDA NDC Directory · JSON-LD · Markdown

Oxcarbazepine

NDC 59651-785 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219241
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsOXCARBAZEPINE (150 mg/1)
Marketing started20261016
Package count1

External sources

Source: openFDA. Public-domain (CC0).