FDA NDC Directory · JSON-LD · Markdown

LOFEXIDINE

NDC 85789-901 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namelofexidine hydrochloride
Labeler / ManufacturerBioCorRx Pharmaceuticals Inc
Marketing categoryNew Drug Application (innovator) · App NDA209229
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLOFEXIDINE HYDROCHLORIDE (.2 mg/1)
Marketing started20260815
Package count2

External sources

Source: openFDA. Public-domain (CC0).