FDA NDC Directory · JSON-LD · Markdown

Nitisinone

NDC 0254-3022 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerEndo USA, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211041
Dosage form / routeCAPSULE · ORAL
Active ingredientsNITISINONE (10 mg/1)
Marketing started20191004
Package count1

External sources

Source: openFDA. Public-domain (CC0).