NDC 78670-050 – Lucemyra

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

Human Prescription Drug

Product NDC78670-050

Product details

Brand name
Lucemyra
Generic name
lofexidine hydrochloride
Labeler
USWM, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA209229
Marketed since
February 9, 2021
Marketing end
June 30, 2027

Active ingredients

Uses, dosage, side effects and warnings for Lucemyra →

Package NDC codes (2)

Package NDCDescriptionSince
78670-050-361 BOTTLE in 1 CARTON (78670-050-36) / 36 TABLET, FILM COATED in 1 BOTTLEFeb 9, 2021
78670-050-961 BOTTLE in 1 CARTON (78670-050-96) / 96 TABLET, FILM COATED in 1 BOTTLEFeb 9, 2021

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