AMINOCAPROIC ACID

NDC 24658-798 · PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS

Generic nameAMINOCAPROIC ACID

Dosage formTABLET

RouteORAL

Active ingredient(s)AMINOCAPROIC ACID

Strength500 mg/1

Pharmacologic classAntifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]

Marketing categoryANDA

Packages

24658-798-30 — 30 TABLET in 1 BOTTLE (24658-798-30)

FDA lists these products with the same active ingredient.

0054-1100 — Aminocaproic Acid, 0054-1110 — Aminocaproic Acid, 0404-9812 — AMINOCAPROIC ACID, 0409-4346 — AMINOCAPROIC ACID, 0517-9120 — Aminocaproic Acid, 0517-9191 — Aminocaproic Acid, 0904-7165 — Aminocaproic acid, 24658-799 — AMINOCAPROIC ACID, 31722-035 — aminocaproic acid, 52817-815 — Aminocaproic Acid, 54288-151 — Aminocaproic acid, 59651-573 — Aminocaproic Acid, 60687-739 — Aminocaproic Acid, 69238-1596 — Aminocaproic acid, 69238-1637 — Aminocaproic acid, 69680-114 — Aminocaproic Acid, 69680-115 — Aminocaproic Acid, 69680-116 — Aminocaproic Acid, 70377-102 — AMINOCAPROIC ACID, 70377-103 — AMINOCAPROIC ACID, +13 more

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