NDC 82804-972 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC82804-972

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA087059
Marketed since
September 25, 2020
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (7)

Package NDCDescriptionSince
82804-972-00100 TABLET in 1 BOTTLE (82804-972-00)Feb 13, 2025
82804-972-111000 TABLET in 1 BOTTLE (82804-972-11)Feb 13, 2025
82804-972-3030 TABLET in 1 BOTTLE (82804-972-30)Feb 13, 2025
82804-972-55500 TABLET in 1 BOTTLE (82804-972-55)Feb 13, 2025
82804-972-6060 TABLET in 1 BOTTLE (82804-972-60)Feb 13, 2025
82804-972-72120 TABLET in 1 BOTTLE (82804-972-72)Feb 13, 2025
82804-972-9090 TABLET in 1 BOTTLE (82804-972-90)Feb 13, 2025

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