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Metaxalone

NDC 0115-1745 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040486
Dosage form / routeTABLET · ORAL
Active ingredientsMETAXALONE (400 mg/1)
Marketing started20160526
Package count1

External sources

Source: openFDA. Public-domain (CC0).