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Metaxalone

NDC 0904-6831 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA207466
Dosage form / routeTABLET · ORAL
Active ingredientsMETAXALONE (800 mg/1)
Marketing started20170831
Package count2

External sources

Source: openFDA. Public-domain (CC0).