NDC 71335-2887 – Spironolactone

Spironolactone 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2887

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA089424
Marketed since
July 23, 1986
Listing expires
December 31, 2027
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (1)

Package NDCDescriptionSince
71335-2887-1100 TABLET, FILM COATED in 1 BOTTLE (71335-2887-1)Oct 28, 2025

Other Spironolactone products