NDC 71335-1976 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1976

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
71335-1976-045 TABLET in 1 BOTTLE (71335-1976-0)Dec 21, 2021
71335-1976-130 TABLET in 1 BOTTLE (71335-1976-1)Oct 15, 2021
71335-1976-260 TABLET in 1 BOTTLE (71335-1976-2)Dec 21, 2021
71335-1976-390 TABLET in 1 BOTTLE (71335-1976-3)Dec 3, 2021
71335-1976-428 TABLET in 1 BOTTLE (71335-1976-4)Dec 21, 2021
71335-1976-556 TABLET in 1 BOTTLE (71335-1976-5)Dec 21, 2021
71335-1976-6100 TABLET in 1 BOTTLE (71335-1976-6)Dec 21, 2021
71335-1976-77 TABLET in 1 BOTTLE (71335-1976-7)Dec 21, 2021
71335-1976-814 TABLET in 1 BOTTLE (71335-1976-8)Dec 21, 2021
71335-1976-9120 TABLET in 1 BOTTLE (71335-1976-9)Dec 21, 2021

Other Hydrochlorothiazide products