NDC 42799-921 – Bisoprolol Fumarate and Hydrochlorothiazide

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

Human Prescription Drug

Product NDC42799-921

Product details

Brand name
Bisoprolol Fumarate and Hydrochlorothiazide
Generic name
Bisoprolol Fumarate and Hydrochlorothiazide
Labeler
Edenbridge Pharmaceuticals LLC.
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 (3)

Package NDCDescriptionSince
42799-921-01100 TABLET, FILM COATED in 1 BOTTLE (42799-921-01)Apr 30, 2019
42799-921-02500 TABLET, FILM COATED in 1 BOTTLE (42799-921-02)Apr 30, 2019
42799-921-3030 TABLET, FILM COATED in 1 BOTTLE (42799-921-30)Apr 30, 2019

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