NDC 71335-2674 – Spironolactone and Hydrochlorothiazide

Spironolactone 25 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2674

Product details

Brand name
Spironolactone and Hydrochlorothiazide
Generic name
Spironolactone and Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA089534
Marketed since
July 2, 1987
Listing expires
December 31, 2026
Pharmacologic class
Aldosterone Antagonist; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone and Hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2674-1100 TABLET in 1 BOTTLE (71335-2674-1)Jun 26, 2025
71335-2674-230 TABLET in 1 BOTTLE (71335-2674-2)Jun 26, 2025
71335-2674-360 TABLET in 1 BOTTLE (71335-2674-3)Jun 26, 2025

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