Tranexamic Acid

Product NDC

68084-929

11-digit product format

680840929

Labeler code

68084

Product ID

68084-929_98f71f3f-db32-5cc2-e053-2995a90aaba9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Tranexamic Acid

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA202093

Marketing category

ANDA

Marketing start

2015-12-18

Marketing end

2020-05-31

Substance

TRANEXAMIC ACID

Active strength

650 mg/1

Pharmacologic classes

Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record