NDC 71335-2616 – Bisoprolol Fumarate and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC71335-2616

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 (3)

Package NDCDescriptionSince
71335-2616-1100 TABLET, FILM COATED in 1 BOTTLE (71335-2616-1)May 29, 2025
71335-2616-230 TABLET, FILM COATED in 1 BOTTLE (71335-2616-2)May 29, 2025
71335-2616-390 TABLET, FILM COATED in 1 BOTTLE (71335-2616-3)May 29, 2025

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