Tranexamic Acid

Product NDC

39822-1001

11-digit product format

398221001

Labeler code

39822

Product ID

39822-1001_1eaef83b-8586-4c20-a776-e9f91656f5e8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tranexamic Acid

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS

Labeler

XGen Pharmaceuticals DJB, Inc.

Application

ANDA201580

Marketing category

ANDA

Marketing start

2012-05-18

Marketing end

0000-00-00

Substance

TRANEXAMIC ACID

Active strength

100 mg/mL

Pharmacologic classes

Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record