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risedronate sodium

NDC 47335-667 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090886
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRISEDRONATE SODIUM HEMI-PENTAHYDRATE (30 mg/1)
Marketing started20151130
Package count4

External sources

Source: openFDA. Public-domain (CC0).