NDC 69584-852 – Spironolactone

Spironolactone 25 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC69584-852

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 (5)

Package NDCDescriptionSince
69584-852-0990 TABLET, COATED in 1 BOTTLE (69584-852-09)Feb 17, 2026
69584-852-10100 TABLET, COATED in 1 BOTTLE (69584-852-10)Jan 4, 2021
69584-852-50500 TABLET, COATED in 1 BOTTLE (69584-852-50)Jan 4, 2021
69584-852-901000 TABLET, COATED in 1 BOTTLE (69584-852-90)Jan 4, 2021
69584-852-922500 TABLET, COATED in 1 BOTTLE (69584-852-92)Jan 4, 2021

Other Spironolactone products