NDC 71335-0269 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0269

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202556
Marketed since
April 10, 2013
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0269-0120 TABLET in 1 BOTTLE (71335-0269-0)Feb 9, 2022
71335-0269-1100 TABLET in 1 BOTTLE (71335-0269-1)Feb 9, 2022
71335-0269-230 TABLET in 1 BOTTLE (71335-0269-2)Feb 9, 2022
71335-0269-37 TABLET in 1 BOTTLE (71335-0269-3)Feb 9, 2022
71335-0269-414 TABLET in 1 BOTTLE (71335-0269-4)Feb 9, 2022
71335-0269-560 TABLET in 1 BOTTLE (71335-0269-5)Feb 9, 2022
71335-0269-62 TABLET in 1 BOTTLE (71335-0269-6)Feb 9, 2022
71335-0269-790 TABLET in 1 BOTTLE (71335-0269-7)Feb 9, 2022
71335-0269-84 TABLET in 1 BOTTLE (71335-0269-8)Feb 9, 2022
71335-0269-98 TABLET in 1 BOTTLE (71335-0269-9)Feb 9, 2022

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