FDA NDC Directory · JSON-LD · Markdown

SUNOSI

NDC 81968-351 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namesolriamfetol
Labeler / ManufacturerAxsome Therapeutics, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA211230
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsSOLRIAMFETOL (150 mg/1)
Marketing started20190618
Package count3

External sources

Source: openFDA. Public-domain (CC0).