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Tranexamic Acid

NDC 25021-415 · Sagent Pharmaceuticals

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic nameTranexamic Acid
Dosage formINJECTION, SOLUTION
RouteINTRAVENOUS
Active ingredient(s)TRANEXAMIC ACID
Strength100 mg/mL
Pharmacologic classAntifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
Marketing categoryANDA

Packages

25021-415-10 — 10 VIAL in 1 CARTON (25021-415-10) / 10 mL in 1 VIAL

25021-415-66 — 10 VIAL in 1 CARTON (25021-415-66) / 10 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0013-1114 — tranexamic acid, 0591-3720 — 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, 25021-418 — 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 August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.