NDC 71335-0652 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0652

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
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 (10)

Package NDCDescriptionSince
71335-0652-08 TABLET in 1 BOTTLE (71335-0652-0)Dec 27, 2021
71335-0652-1100 TABLET in 1 BOTTLE (71335-0652-1)Jan 21, 2021
71335-0652-230 TABLET in 1 BOTTLE (71335-0652-2)Mar 9, 2018
71335-0652-37 TABLET in 1 BOTTLE (71335-0652-3)Apr 11, 2018
71335-0652-414 TABLET in 1 BOTTLE (71335-0652-4)Mar 15, 2021
71335-0652-560 TABLET in 1 BOTTLE (71335-0652-5)Nov 16, 2021
71335-0652-62 TABLET in 1 BOTTLE (71335-0652-6)Dec 27, 2021
71335-0652-790 TABLET in 1 BOTTLE (71335-0652-7)Mar 14, 2018
71335-0652-84 TABLET in 1 BOTTLE (71335-0652-8)May 10, 2018
71335-0652-96 TABLET in 1 BOTTLE (71335-0652-9)Dec 27, 2021

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