NDC 71335-1713 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC71335-1713

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA203561
Marketed since
January 14, 2019
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (9)

Package NDCDescriptionSince
71335-1713-130 CAPSULE in 1 BOTTLE (71335-1713-1)Jan 15, 2021
71335-1713-210 CAPSULE in 1 BOTTLE (71335-1713-2)Apr 12, 2021
71335-1713-390 CAPSULE in 1 BOTTLE (71335-1713-3)Oct 2, 2020
71335-1713-4100 CAPSULE in 1 BOTTLE (71335-1713-4)Feb 12, 2021
71335-1713-560 CAPSULE in 1 BOTTLE (71335-1713-5)Dec 10, 2024
71335-1713-6120 CAPSULE in 1 BOTTLE (71335-1713-6)Aug 12, 2021
71335-1713-77 CAPSULE in 1 BOTTLE (71335-1713-7)Jul 2, 2021
71335-1713-815 CAPSULE in 1 BOTTLE (71335-1713-8)Dec 10, 2024
71335-1713-914 CAPSULE in 1 BOTTLE (71335-1713-9)Jul 2, 2021

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