NDC 71335-0067 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-0067

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA090510
Marketed since
March 15, 2010
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
71335-0067-130 CAPSULE in 1 BOTTLE (71335-0067-1)Apr 3, 2018
71335-0067-210 CAPSULE in 1 BOTTLE (71335-0067-2)May 29, 2024
71335-0067-390 CAPSULE in 1 BOTTLE (71335-0067-3)Apr 3, 2018
71335-0067-4100 CAPSULE in 1 BOTTLE (71335-0067-4)Aug 12, 2020
71335-0067-560 CAPSULE in 1 BOTTLE (71335-0067-5)May 29, 2024
71335-0067-6120 CAPSULE in 1 BOTTLE (71335-0067-6)Aug 6, 2020
71335-0067-77 CAPSULE in 1 BOTTLE (71335-0067-7)May 29, 2024
71335-0067-815 CAPSULE in 1 BOTTLE (71335-0067-8)May 29, 2024
71335-0067-914 CAPSULE in 1 BOTTLE (71335-0067-9)Mar 5, 2021

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