NDC 50228-111 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50228-111

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203018
Marketed since
July 23, 2014
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
50228-111-101000 TABLET in 1 BOTTLE (50228-111-10)Jul 23, 2014
50228-111-3030 TABLET in 1 BOTTLE (50228-111-30)Jul 23, 2014

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