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tramadol hydrochloride

NDC 64380-791 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202075
Dosage form / routeTABLET · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (50 mg/1)
Marketing started20260727
Package count3

External sources

Source: openFDA. Public-domain (CC0).