NDC 71335-0770 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0770

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078164
Marketed since
September 19, 2007
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (9)

Package NDCDescriptionSince
71335-0770-130 CAPSULE in 1 BOTTLE (71335-0770-1)Apr 13, 2018
71335-0770-210 CAPSULE in 1 BOTTLE (71335-0770-2)May 7, 2018
71335-0770-390 CAPSULE in 1 BOTTLE (71335-0770-3)Apr 10, 2018
71335-0770-4100 CAPSULE in 1 BOTTLE (71335-0770-4)Oct 1, 2018
71335-0770-560 CAPSULE in 1 BOTTLE (71335-0770-5)Oct 15, 2019
71335-0770-6120 CAPSULE in 1 BOTTLE (71335-0770-6)Aug 13, 2019
71335-0770-77 CAPSULE in 1 BOTTLE (71335-0770-7)Apr 11, 2019
71335-0770-815 CAPSULE in 1 BOTTLE (71335-0770-8)Apr 11, 2019
71335-0770-914 CAPSULE in 1 BOTTLE (71335-0770-9)Oct 7, 2024

Other Hydrochlorothiazide products