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Eslicarbazepine Acetate

NDC 67877-588 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211199
Dosage form / routeTABLET · ORAL
Active ingredientsESLICARBAZEPINE ACETATE (800 mg/1)
Marketing started20250506
Package count1

External sources

Source: openFDA. Public-domain (CC0).