NDC 71335-2589 – Bisoprolol Fumarate and Hydrochlorothiazide

Bisoprolol Fumarate 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2589

Product details

Brand name
Bisoprolol Fumarate and Hydrochlorothiazide
Generic name
Bisoprolol Fumarate and Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215995
Marketed since
January 26, 2022
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic; beta-Adrenergic Blocker

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
71335-2589-130 TABLET, FILM COATED in 1 BOTTLE (71335-2589-1)Jun 4, 2025
71335-2589-290 TABLET, FILM COATED in 1 BOTTLE (71335-2589-2)Jun 4, 2025
71335-2589-328 TABLET, FILM COATED in 1 BOTTLE (71335-2589-3)Jun 4, 2025
71335-2589-4100 TABLET, FILM COATED in 1 BOTTLE (71335-2589-4)Jun 4, 2025

Other Bisoprolol fumarate and hydrochlorothiazide products