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TRAMADOL HYDROCHLORIDE

NDC 27808-301 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCranbury Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091498
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTRAMADOL HYDROCHLORIDE (50 mg/1)
Marketing started20241222
Package count3

External sources

Source: openFDA. Public-domain (CC0).