NDC 70771-1761 – Bisoprolol Fumarate and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC70771-1761

Product details

Brand name
Bisoprolol Fumarate and Hydrochlorothiazide
Generic name
Bisoprolol fumarate and hydrochlorothiazide
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215666
Marketed since
March 1, 2023
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
70771-1761-1100 TABLET, FILM COATED in 1 BOTTLE (70771-1761-1)Mar 1, 2023
70771-1761-330 TABLET, FILM COATED in 1 BOTTLE (70771-1761-3)Mar 1, 2023
70771-1761-5500 TABLET, FILM COATED in 1 BOTTLE (70771-1761-5)Mar 1, 2023

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