Skip to main content

spironolactone

NDC 0904-6927 · Major Pharmaceuticals

Generic namespironolactone
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)SPIRONOLACTONE
Strength25 mg/1
Pharmacologic classAldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
Marketing categoryANDA

Packages

0904-6927-61 — 100 BLISTER PACK in 1 CARTON (0904-6927-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0025-1001 — spironolactone, 0025-1031 — spironolactone, 0025-1041 — spironolactone, 0378-0243 — spironolactone, 0378-0403 — spironolactone and hydrochlorothiazide, 0378-0437 — spironolactone, 0378-2146 — spironolactone, 0574-1133 — spironolactone, 0615-8451 — SPIRONOLACTONE, 0615-8452 — SPIRONOLACTONE, 16729-225 — spironolactone, 16729-226 — spironolactone, 16729-227 — spironolactone, 17856-1133 — spironolactone, 31722-094 — spironolactone, 31722-095 — spironolactone, 31722-096 — spironolactone, 31722-691 — spironolactone, 42292-017 — spironolactone and hydrochlorothiazide, 42708-101 — spironolactone, +165 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.