NDC 23155-009 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-009

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA085182
Marketed since
January 15, 2015
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
23155-009-01100 TABLET in 1 BOTTLE (23155-009-01)Jan 15, 2015
23155-009-05500 TABLET in 1 BOTTLE (23155-009-05)Jan 15, 2015
23155-009-101000 TABLET in 1 BOTTLE (23155-009-10)Jan 15, 2015
23155-009-185000 TABLET in 1 BOTTLE (23155-009-18)Feb 1, 2015

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