FDA NDC Directory · JSON-LD · Markdown

OXCARBAZEPINE

NDC 70518-4664 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA078069
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (600 mg/1)
Marketing started20260520
Package count2

External sources

Source: openFDA. Public-domain (CC0).