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TOLMETIN SODIUM

NDC 16571-825 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nametolmetin sodium
Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074473
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsTOLMETIN SODIUM (600 mg/1)
Marketing started20230411
Marketing ended20260531
Package count1

External sources

Source: openFDA. Public-domain (CC0).