FDA NDC Directory · JSON-LD · Markdown

Flucytosine

NDC 23155-861 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212632
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUCYTOSINE (500 mg/1)
Marketing started20230625
Package count2

External sources

Source: openFDA. Public-domain (CC0).