NDC 82804-031 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-031

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
82804-031-3030 TABLET in 1 BOTTLE (82804-031-30)Oct 24, 2023
82804-031-6060 TABLET in 1 BOTTLE (82804-031-60)Oct 24, 2023
82804-031-9090 TABLET in 1 BOTTLE (82804-031-90)Oct 24, 2023

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