FDA NDC Directory · JSON-LD · Markdown

GEMTESA

NDC 73336-075 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namevibegron
Labeler / ManufacturerSumitomo Pharma America, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA213006
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsVIBEGRON (75 mg/1)
Marketing started20201229
Package count3

External sources

Source: openFDA. Public-domain (CC0).