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Tramadol Hydrochloride

NDC 72888-080 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerAdvagen Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA208708
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (50 mg/1)
Marketing started20230724
Package count3

External sources

Source: openFDA. Public-domain (CC0).