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Oxcarbazepine

NDC 0615-8448 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNCS HealthCare of KY, LLC dba Vangard Labs
Marketing categoryAbbreviated NDA (generic) · App ANDA215939
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsOXCARBAZEPINE (300 mg/1)
Marketing started20220111
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).