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Methocarbamol

NDC 80425-0275 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx Pharmacy of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090200
Dosage form / routeTABLET · ORAL
Active ingredientsMETHOCARBAMOL (500 mg/1)
Marketing started20230217
Package count3

External sources

Source: openFDA. Public-domain (CC0).