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Tramadol Hydrochloride

NDC 68071-4119 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076003
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (50 mg/1)
Marketing started20101115
Package count8

External sources

Source: openFDA. Public-domain (CC0).