NDC 29300-129 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-129

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
August 15, 2008
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
29300-129-01100 TABLET in 1 BOTTLE (29300-129-01)Jul 2, 2009
29300-129-05500 TABLET in 1 BOTTLE (29300-129-05)Jul 2, 2009
29300-129-101000 TABLET in 1 BOTTLE (29300-129-10)Jul 2, 2009
29300-129-505000 TABLET in 1 BOTTLE (29300-129-50)Jul 2, 2009

Recalls mentioning this NDC

Other Hydrochlorothiazide products