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Methocarbamol

NDC 80425-0020 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209312
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETHOCARBAMOL (750 mg/1)
Marketing started20180702
Package count3

External sources

Source: openFDA. Public-domain (CC0).