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Diclofenac Sodium

NDC 68001-280 · HUMAN PRESCRIPTION DRUG · TABLET, DELAYED RELEASE

Labeler / ManufacturerBluePoint Laboratories
Marketing categoryAbbreviated NDA (generic) · App ANDA090066
Dosage form / routeTABLET, DELAYED RELEASE · ORAL
Active ingredientsDICLOFENAC SODIUM (50 mg/1)
Marketing started20151221
Package count3

External sources

Source: openFDA. Public-domain (CC0).