Tranexamic Acid
- Product NDC
- 17478-017
- 11-digit product format
- 174780017
- Labeler code
- 17478
- Product ID
- 17478-017_bf142dfd-6b01-4f16-8bb5-a1c5c2e05c08
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tranexamic Acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA206634
- Marketing category
- ANDA
- Marketing start
- 2016-06-09
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 17478-017-10 | 17478001710 | 5 AMPULE in 1 CARTON (17478-017-10) > 10 mL in 1 AMPULE | 5 ampule | 2016-06-09 | 0000-00-00 | No | No | Current |