FDA NDC Directory · JSON-LD · Markdown

Attruby

NDC 82228-712 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameacoramidis hydrochloride
Labeler / ManufacturerBridgeBio Pharma, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA216540
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsACORAMIDIS HYDROCHLORIDE (356 mg/1)
Marketing started20241122
Package count1

External sources

Source: openFDA. Public-domain (CC0).