NDC 53489-143 – Spironolactone

Spironolactone 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC53489-143

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA089424
Marketed since
July 23, 1986
Marketing end
February 28, 2029
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (3)

Package NDCDescriptionSince
53489-143-01100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01)Jul 23, 1986
53489-143-05500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05)Jul 23, 1986
53489-143-101000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)Jul 23, 1996

Recalls mentioning this NDC

Other Spironolactone products