Tranexamic Acid

Product NDC
66993-121
11-digit product format
669930121
Labeler code
66993
Product ID
66993-121_a2b02c92-a449-4624-9936-423a9c0993e2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Tranexamic Acid
Dosage form
TABLET
Route
ORAL
Labeler
Prasco Laboratories
Application
NDA022430
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2010-05-17
Marketing end
0000-00-00
Substance
TRANEXAMIC ACID
Active strength
650 mg/1
Pharmacologic classes
Antifibrinolytic Agent [EPC],Decreased Fibrinolysis [PE]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66993-121-30EA - Each66993-12195b00956-f654-433e-ad26-d571d27fb00712014-01-04