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Diclofenac Potassium

NDC 72819-151 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namediclofenac potassium
Labeler / ManufacturerArchis Pharma LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075463
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDICLOFENAC POTASSIUM (50 mg/1)
Marketing started20210915
Package count1

External sources

Source: openFDA. Public-domain (CC0).