FDA NDC Directory · JSON-LD · Markdown

Oxcarbazepine

NDC 70518-3940 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215939
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (150 mg/1)
Marketing started20231206
Package count2

External sources

Source: openFDA. Public-domain (CC0).