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Risedronate Sodium

NDC 60505-3097 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA090877
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsRISEDRONATE SODIUM (150 mg/1)
Marketing started20140611
Package count2

External sources

Source: openFDA. Public-domain (CC0).