NDC 71335-2366 – Spironolactone

Spironolactone 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2366

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
Listing expires
December 31, 2027
Pharmacologic class
Aldosterone Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Spironolactone →

Package NDC codes (9)

Package NDCDescriptionSince
71335-2366-130 TABLET in 1 BOTTLE, PLASTIC (71335-2366-1)Apr 30, 2024
71335-2366-260 TABLET in 1 BOTTLE, PLASTIC (71335-2366-2)Apr 30, 2024
71335-2366-390 TABLET in 1 BOTTLE, PLASTIC (71335-2366-3)Apr 30, 2024
71335-2366-414 TABLET in 1 BOTTLE, PLASTIC (71335-2366-4)Apr 30, 2024
71335-2366-5100 TABLET in 1 BOTTLE, PLASTIC (71335-2366-5)Apr 30, 2024
71335-2366-67 TABLET in 1 BOTTLE, PLASTIC (71335-2366-6)Apr 30, 2024
71335-2366-710 TABLET in 1 BOTTLE, PLASTIC (71335-2366-7)Apr 30, 2024
71335-2366-8180 TABLET in 1 BOTTLE, PLASTIC (71335-2366-8)Apr 30, 2024
71335-2366-945 TABLET in 1 BOTTLE, PLASTIC (71335-2366-9)Apr 30, 2024

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