NDC 29300-485 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC29300-485

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Unichem Pharmaceuticals (USA), Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
April 3, 2025
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
29300-485-01100 TABLET in 1 BOTTLE (29300-485-01)Jun 12, 2025
29300-485-101000 TABLET in 1 BOTTLE (29300-485-10)Jun 12, 2025

Recalls mentioning this NDC

Other Hydrochlorothiazide products