NDC 29300-188 – Bisoprolol fumarate and hydrochlorothiazide

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

Human Prescription Drug 1 recall

Product NDC29300-188

Product details

Brand name
Bisoprolol fumarate and hydrochlorothiazide
Generic name
Bisoprolol fumarate and hydrochlorothiazide
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA079106
Marketed since
October 12, 2010
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
29300-188-01100 TABLET in 1 BOTTLE, PLASTIC (29300-188-01)Oct 12, 2010
29300-188-05500 TABLET in 1 BOTTLE, PLASTIC (29300-188-05)Oct 12, 2010
29300-188-101000 TABLET in 1 BOTTLE, PLASTIC (29300-188-10)Oct 12, 2010
29300-188-1330 TABLET in 1 BOTTLE, PLASTIC (29300-188-13)Oct 12, 2010

Recalls mentioning this NDC

Other Bisoprolol fumarate and hydrochlorothiazide products