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spironolactone

NDC 51655-636 · Northwind Health Company, LLC

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

Packages

51655-636-26 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-636-26)

51655-636-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-636-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6908 — SPIRONOLACTONE, 50090-6909 — SPIRONOLACTONE, 50090-7082 — SPIRONOLACTONE, 50090-7083 — SPIRONOLACTONE, 50090-7797 — Spironolactone, 51079-103 — spironolactone, 51079-979 — spironolactone, 51079-980 — spironolactone, 51655-153 — spironolactone, 51655-344 — spironolactone, 51655-861 — spironolactone, 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, +165 more

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