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Metaxalone

NDC 85509-2341 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPHOENIX RX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203695
Dosage form / routeTABLET · ORAL
Active ingredientsMETAXALONE (800 mg/1)
Marketing started20170619
Package count5

External sources

Source: openFDA. Public-domain (CC0).