FDA NDC Directory · JSON-LD · Markdown

Flucytosine

NDC 0904-6835 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA204652
Dosage form / routeCAPSULE · ORAL
Active ingredientsFLUCYTOSINE (500 mg/1)
Marketing started20170707
Package count1

External sources

Source: openFDA. Public-domain (CC0).