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SPIRONOLACTONE

NDC 53489-329 · Sun Pharmaceutical Industries, Inc.

Generic nameSPIRONOLACTONE
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)SPIRONOLACTONE
Strength100 mg/1
Pharmacologic classAldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
Marketing categoryANDA

Packages

53489-329-01 — 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-01)

53489-329-02 — 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-02)

53489-329-03 — 250 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-03)

53489-329-05 — 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-05)

53489-329-10 — 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-329-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 53489-328 — 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, 59746-216 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels