NDC 69584-853 – Spironolactone

Spironolactone 50 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC69584-853

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA040750
Marketed since
January 4, 2021
Listing expires
December 31, 2027
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (4)

Package NDCDescriptionSince
69584-853-0990 TABLET, COATED in 1 BOTTLE (69584-853-09)Feb 17, 2026
69584-853-10100 TABLET, COATED in 1 BOTTLE (69584-853-10)Jan 4, 2021
69584-853-50500 TABLET, COATED in 1 BOTTLE (69584-853-50)Jan 4, 2021
69584-853-901000 TABLET, COATED in 1 BOTTLE (69584-853-90)Apr 1, 2024

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