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Diclofenac Potassium

NDC 67046-1522 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Generic namediclofenac potassium
Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075229
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsDICLOFENAC POTASSIUM (50 mg/1)
Marketing started20250224
Package count1

External sources

Source: openFDA. Public-domain (CC0).