FDA NDC Directory · JSON-LD · Markdown

Dipyridamole

NDC 68382-188 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040874
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDIPYRIDAMOLE (50 mg/1)
Marketing started20080522
Package count4

External sources

Source: openFDA. Public-domain (CC0).