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lofexidine hydrochloride

NDC 72205-246 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218699
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLOFEXIDINE HYDROCHLORIDE (.2 mg/1)
Marketing started20250224
Package count2

External sources

Source: openFDA. Public-domain (CC0).