NDC 68462-878 – Bisoprolol Fumarate and Hydrochlorothiazide

Bisoprolol Fumarate 2.5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 2 recalls

Product NDC68462-878

Product details

Brand name
Bisoprolol Fumarate and Hydrochlorothiazide
Generic name
Bisoprolol Fumarate and Hydrochlorothiazide
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215995
Marketed since
January 26, 2022
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for bisoprolol fumarate and hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
68462-878-01100 TABLET, FILM COATED in 1 BOTTLE (68462-878-01)Jan 26, 2022
68462-878-05500 TABLET, FILM COATED in 1 BOTTLE (68462-878-05)Jan 26, 2022
68462-878-3030 TABLET, FILM COATED in 1 BOTTLE (68462-878-30)Jan 26, 2022

Recalls mentioning this NDC

Other bisoprolol fumarate and hydrochlorothiazide products