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SPIRONOLACTONE

NDC 50090-7083 · A-S Medication Solutions

Generic nameSPIRONOLACTONE
Dosage formTABLET
RouteORAL
Active ingredient(s)SPIRONOLACTONE
Strength50 mg/1
Pharmacologic classAldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
Marketing categoryANDA

Packages

50090-7083-0 — 90 TABLET in 1 BOTTLE (50090-7083-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3747 — spironolactone, 50090-6369 — Spironolactone, 50090-6408 — SPIRONOLACTONE, 50090-6432 — SPIRONOLACTONE, 50090-6458 — Spironolactone, 50090-6539 — Spironolactone, 50090-6600 — Spironolactone, 50090-6908 — SPIRONOLACTONE, 50090-6909 — SPIRONOLACTONE, 50090-7082 — SPIRONOLACTONE, 50090-7797 — Spironolactone, 51079-103 — spironolactone, 51079-979 — spironolactone, 51079-980 — spironolactone, 51655-153 — spironolactone, 51655-344 — spironolactone, 51655-636 — spironolactone, 51655-861 — spironolactone, 53489-143 — SPIRONOLACTONE, 53489-144 — Spironolactone and Hydrochlorothiazide, +165 more

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