Drug Atlas

NDC 29300-128 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-128

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

Hydrochlorothiazide 25 mg/1

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (4)

Package NDC	Description	Since
29300-128-01	100 TABLET in 1 BOTTLE (29300-128-01)	Jul 2, 2009
29300-128-05	500 TABLET in 1 BOTTLE (29300-128-05)	Jul 2, 2009
29300-128-10	1000 TABLET in 1 BOTTLE (29300-128-10)	Jul 2, 2009
29300-128-50	5000 TABLET in 1 BOTTLE (29300-128-50)	Jul 2, 2009

Recalls mentioning this NDC

D-1352-2015 Sep 2, 2015 · Class II
Presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothiazide 25 mg tablets.

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