NDC 71335-1769 – Bisoprolol Fumarate and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC71335-1769

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 · ANDA212678
Marketed since
April 30, 2019
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 (4)

Package NDCDescriptionSince
71335-1769-130 TABLET, FILM COATED in 1 BOTTLE (71335-1769-1)Feb 2, 2021
71335-1769-290 TABLET, FILM COATED in 1 BOTTLE (71335-1769-2)Dec 29, 2021
71335-1769-328 TABLET, FILM COATED in 1 BOTTLE (71335-1769-3)Dec 29, 2021
71335-1769-4100 TABLET, FILM COATED in 1 BOTTLE (71335-1769-4)Apr 5, 2024

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