FDA NDC Directory · JSON-LD · Markdown

Oxcarbazepine

NDC 71205-411 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077802
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (150 mg/1)
Marketing started20071009
Package count3

External sources

Source: openFDA. Public-domain (CC0).