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Tramadol Hydrochloride

NDC 33342-271 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA209404
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (300 mg/1)
Marketing started20250131
Package count3

External sources

Source: openFDA. Public-domain (CC0).