Spironolactone

NDC 16729-226 · Accord Healthcare, 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

16729-226-01 — 100 TABLET, FILM COATED in 1 BOTTLE (16729-226-01)

16729-226-16 — 500 TABLET, FILM COATED in 1 BOTTLE (16729-226-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0025-1041 — spironolactone, 0378-0243 — spironolactone, 0378-0403 — spironolactone and hydrochlorothiazide, 0378-0437 — spironolactone, 0378-2146 — spironolactone, 0574-1133 — spironolactone, 0615-8451 — SPIRONOLACTONE, 0615-8452 — SPIRONOLACTONE, 0904-6927 — spironolactone, 16729-225 — 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, 42708-101 — spironolactone, 42708-126 — 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.