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SPIRONOLACTONE

NDC 53489-328 · Sun Pharmaceutical Industries, Inc.

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

Packages

53489-328-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-01)

53489-328-02 — 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-02)

53489-328-03 — 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-03)

53489-328-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-05)

53489-328-07 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-07)

53489-328-10 — 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-328-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 53489-329 — SPIRONOLACTONE, 53746-511 — Spironolactone, 53746-514 — Spironolactone, 53746-515 — Spironolactone, 54348-340 — SPIRONOLACTONE, 55154-3556 — spironolactone, 55154-5517 — spironolactone, 59651-426 — SPIRONOLACTONE, 59651-427 — SPIRONOLACTONE, 59651-428 — 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.