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SPIRONOLACTONE

NDC 59651-426 · Aurobindo Pharma Limited

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

Packages

59651-426-01 — 100 TABLET in 1 BOTTLE (59651-426-01)

59651-426-05 — 500 TABLET in 1 BOTTLE (59651-426-05)

59651-426-99 — 1000 TABLET in 1 BOTTLE (59651-426-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

53489-143 — SPIRONOLACTONE, 53489-144 — Spironolactone and Hydrochlorothiazide, 53489-328 — SPIRONOLACTONE, 53489-329 — SPIRONOLACTONE, 53746-511 — Spironolactone, 53746-514 — Spironolactone, 53746-515 — Spironolactone, 54348-340 — SPIRONOLACTONE, 55154-3556 — spironolactone, 55154-5517 — spironolactone, 59651-427 — SPIRONOLACTONE, 59651-428 — SPIRONOLACTONE, 59746-216 — spironolactone, 59746-217 — spironolactone, 59746-218 — spironolactone, 60687-465 — Spironolactone, 60687-476 — Spironolactone, 60687-487 — Spironolactone, 63187-841 — spironolactone, 63187-861 — 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.