FDA NDC Directory · JSON-LD · Markdown

Oxcarbazepine

NDC 90096-172 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZameer Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218341
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (300 mg/1)
Marketing started20260706
Package count1

External sources

Source: openFDA. Public-domain (CC0).