FDA NDC Directory · JSON-LD · Markdown

LYTGOBI

NDC 64842-0128 · HUMAN PRESCRIPTION DRUG · KIT

Labeler / ManufacturerTAIHO PHARMACEUTICAL CO., LTD.
Marketing categoryNew Drug Application (innovator) · App NDA214801
Dosage form / routeKIT
Active ingredients—
Marketing started20260601
Package count1

External sources

Source: openFDA. Public-domain (CC0).