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Diclofenac Sodium

NDC 70512-784 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerSOLA Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075185
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDICLOFENAC SODIUM (75 mg/1)
Marketing started20251114
Package count1

External sources

Source: openFDA. Public-domain (CC0).