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Methocarbamol

NDC 73352-510 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerTrifluent Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA200958
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETHOCARBAMOL (1000 mg/1)
Marketing started20250210
Package count1

External sources

Source: openFDA. Public-domain (CC0).