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nisoldipine

NDC 23155-977 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216606
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsNISOLDIPINE (17 mg/1)
Marketing started20260801
Package count1

External sources

Source: openFDA. Public-domain (CC0).