Tranexamic Acid

NDC 0591-3720 · Actavis Pharma, Inc.

Generic nameTranexamic Acid

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)TRANEXAMIC ACID

Strength650 mg/1

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

Marketing categoryANDA

Packages

0591-3720-30 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3720-30)

FDA lists these products with the same active ingredient.

0013-1114 — tranexamic acid, 14593-318 — Tranexamic Acid, 14789-115 — Tranexamic Acid, 23155-166 — Tranexamic Acid, 23155-524 — Tranexamic Acid, 23155-909 — Tranexamic Acid, 23155-910 — Tranexamic Acid, 25021-415 — Tranexamic Acid, 25021-418 — Tranexamic Acid, 39822-1000 — Tranexamic Acid, 42571-189 — TRANEXAMIC ACID, 42571-314 — TRANEXAMIC ACID, 43066-008 — tranexamic acid, 50268-772 — Tranexamic Acid, 51662-1532 — TRANEXAMIC ACID, 51754-0108 — tranexamic acid, 55150-188 — Tranexamic Acid, 59651-839 — TRANEXAMIC ACID, 60505-6169 — tranexamic acid, 60687-750 — Tranexamic Acid, +27 more

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