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Tramadol Hydrochloride and Acetaminophen

NDC 65862-922 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207152
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACETAMINOPHEN (325 mg/1)
TRAMADOL HYDROCHLORIDE (37.5 mg/1)
Marketing started20170322
Package count5

External sources

Source: openFDA. Public-domain (CC0).