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Diclofenac Potassium

NDC 67877-772 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216635
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsDICLOFENAC POTASSIUM (50 mg/1)
Marketing started20221024
Package count1

External sources

Source: openFDA. Public-domain (CC0).