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Metaxalone

NDC 0527-1435 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerLannett Company, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204770
Dosage form / routeTABLET · ORAL
Active ingredientsMETAXALONE (800 mg/1)
Marketing started20161122
Package count2

External sources

Source: openFDA. Public-domain (CC0).