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