FDA NDC Directory · JSON-LD · Markdown

voriconazole

NDC 43386-088 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLupin Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207371
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVORICONAZOLE (50 mg/1)
Marketing started20160524
Package count1

External sources

Source: openFDA. Public-domain (CC0).