NDC 63629-7782 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-7782

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202556
Marketed since
April 18, 2013
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
63629-7782-130 TABLET in 1 BOTTLE (63629-7782-1)Nov 18, 2021
63629-7782-290 TABLET in 1 BOTTLE (63629-7782-2)Apr 14, 2021
63629-7782-314 TABLET in 1 BOTTLE (63629-7782-3)Sep 23, 2019
63629-7782-4100 TABLET in 1 BOTTLE (63629-7782-4)Jan 22, 2021

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