FDA NDC Directory · JSON-LD · Markdown

Tapentadol Hydrochloride

NDC 70954-801 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerANI Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219119
Dosage form / routeSOLUTION · ORAL
Active ingredientsTAPENTADOL HYDROCHLORIDE (20 mg/mL)
Marketing started20260713
Package count2

External sources

Source: openFDA. Public-domain (CC0).