FDA NDC Directory · JSON-LD · Markdown

Lofexidine

NDC 71921-250 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218613
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsLOFEXIDINE HYDROCHLORIDE (.18 mg/1)
Marketing started20240821
Package count2

External sources

Source: openFDA. Public-domain (CC0).