FDA NDC Directory · JSON-LD · Markdown

CEVIMELINE

NDC 69452-316 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameCEVIMELINE HYDROCHLORIDE
Labeler / ManufacturerBionpharma Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA218290
Dosage form / routeCAPSULE · ORAL
Active ingredientsCEVIMELINE HYDROCHLORIDE (30 mg/1)
Marketing started20240117
Package count1

External sources

Source: openFDA. Public-domain (CC0).