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NDC 70515-501 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namenisoldipine
Labeler / ManufacturerCovis Pharma US, Inc
Marketing categoryNew Drug Application (innovator) · App NDA020356
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNISOLDIPINE (17 mg/1)
Marketing started20170203
Package count1

External sources

Source: openFDA. Public-domain (CC0).