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Tramadol Hydrochloride

NDC 80425-0588 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075968
Dosage form / routeTABLET · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (50 mg/1)
Marketing started20260626
Package count8

External sources

Source: openFDA. Public-domain (CC0).