NDC 85789-801 – Lucemyra

Lofexidine Hydrochloride .2 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC85789-801

Product details

Brand name
Lucemyra
Generic name
lofexidine hydrochloride
Labeler
BioCorRx Pharmaceuticals Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA209229
Marketed since
August 15, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lucemyra →

Package NDC codes (2)

Package NDCDescriptionSince
85789-801-3636 TABLET, FILM COATED in 1 BOTTLE (85789-801-36)Aug 15, 2026
85789-801-9696 TABLET, FILM COATED in 1 BOTTLE (85789-801-96)Aug 15, 2026

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