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SPIRONOLACTONE

NDC 50090-0136 · A-S Medication Solutions

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

Packages

50090-0136-0 — 100 TABLET in 1 BOTTLE, PLASTIC (50090-0136-0)

50090-0136-1 — 30 TABLET in 1 BOTTLE, PLASTIC (50090-0136-1)

50090-0136-6 — 90 TABLET in 1 BOTTLE, PLASTIC (50090-0136-6)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42708-101 — spironolactone, 42708-126 — Spironolactone, 43063-832 — spironolactone, 43063-835 — spironolactone, 43063-974 — spironolactone, 46287-020 — CaroSpir, 48433-087 — spironolactone, 48433-088 — spironolactone, 48433-089 — spironolactone, 48433-090 — spironolactone and hydrochlorothiazide, 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, +165 more

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