NDC 59651-678 – Bisoprolol Fumarate and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC59651-678

Product details

Brand name
Bisoprolol Fumarate and Hydrochlorothiazide
Generic name
Bisoprolol Fumarate and Hydrochlorothiazide
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA217922
Marketed since
January 21, 2026
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 (3)

Package NDCDescriptionSince
59651-678-01100 TABLET, FILM COATED in 1 BOTTLE (59651-678-01)Jan 21, 2026
59651-678-05500 TABLET, FILM COATED in 1 BOTTLE (59651-678-05)Jan 21, 2026
59651-678-3030 TABLET, FILM COATED in 1 BOTTLE (59651-678-30)Jan 21, 2026

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