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Spironolactone

NDC 42708-101 · QPharma, Inc.

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

Packages

42708-101-30 — 30 TABLET, FILM COATED in 1 BOTTLE (42708-101-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16729-225 — spironolactone, 16729-226 — spironolactone, 16729-227 — spironolactone, 17089-260 — amiloride - apis mellifera - berberis vulgaris fruit - hieracium pilosella flowering top - hydrochlorothiazide - solidago virgaurea flowering top - spironolactone - sus scrofa pituitary gland -, 17856-1133 — spironolactone, 31722-094 — spironolactone, 31722-095 — spironolactone, 31722-096 — spironolactone, 31722-691 — spironolactone, 42292-017 — spironolactone and hydrochlorothiazide, 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, 50090-0136 — SPIRONOLACTONE, +166 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.