NDC 71335-0595 – Bisoprolol fumarate and hydrochlorothiazide

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

Human Prescription Drug

Product NDC71335-0595

Product details

Brand name
Bisoprolol fumarate and hydrochlorothiazide
Generic name
Bisoprolol fumarate and hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079106
Marketed since
October 12, 2010
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
71335-0595-130 TABLET in 1 BOTTLE, PLASTIC (71335-0595-1)Jun 25, 2018
71335-0595-290 TABLET in 1 BOTTLE, PLASTIC (71335-0595-2)Mar 19, 2019
71335-0595-328 TABLET in 1 BOTTLE, PLASTIC (71335-0595-3)May 23, 2024
71335-0595-4100 TABLET in 1 BOTTLE, PLASTIC (71335-0595-4)Jul 19, 2023

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