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DICLOFENAC SODIUM

NDC 70518-4694 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA075281
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDICLOFENAC SODIUM (50 mg/1)
Marketing started20260708
Package count1

External sources

Source: openFDA. Public-domain (CC0).