NDC 63629-1064 – Spironolactone

Spironolactone 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC63629-1064

Product details

Brand name
Spironolactone
Generic name
Spironolactone
Labeler
Bryant Ranch Prepack
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 (6)

Package NDCDescriptionSince
63629-1064-130 TABLET in 1 BOTTLE, PLASTIC (63629-1064-1)Sep 9, 2026
63629-1064-260 TABLET in 1 BOTTLE, PLASTIC (63629-1064-2)Sep 21, 2020
63629-1064-390 TABLET in 1 BOTTLE, PLASTIC (63629-1064-3)Sep 21, 2020
63629-1064-4100 TABLET in 1 BOTTLE, PLASTIC (63629-1064-4)Aug 28, 2023
63629-1064-545 TABLET in 1 BOTTLE, PLASTIC (63629-1064-5)Sep 9, 2026
63629-1064-6180 TABLET in 1 BOTTLE, PLASTIC (63629-1064-6)Sep 9, 2026

Recalls mentioning this NDC

Other Spironolactone products