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Diclofenac Sodium

NDC 60290-082 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerUmedica Laboratories USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219945
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDICLOFENAC SODIUM (25 mg/1)
Marketing started20260215
Package count1

External sources

Source: openFDA. Public-domain (CC0).