NDC 72162-1357 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-1357

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040412
Marketed since
March 29, 2002
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
72162-1357-1100 TABLET in 1 BOTTLE, PLASTIC (72162-1357-1)Feb 5, 2024

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