Tranexamic Acid
- Product NDC
- 60687-750
- 11-digit product format
- 606870750
- Labeler code
- 60687
- Product ID
- 60687-750_4c258bec-ab80-cb54-e063-6394a90a1893
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tranexamic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA203256
- Marketing category
- ANDA
- Marketing start
- 2023-10-01
- Substance
- TRANEXAMIC ACID
- Active strength
- 650 mg/1
- Pharmacologic classes
- Antifibrinolytic Agent [EPC], Decreased Fibrinolysis [PE]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6T84R30KC1 | TRANEXAMIC ACID | 1197-18-8 | TRANEXAMIC ACID |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-750-21 | 60687075021 | 30 BLISTER PACK in 1 CARTON (60687-750-21) / 1 TABLET in 1 BLISTER PACK (60687-750-11) | 30 blister pack | 2023-10-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Tranexamic Acid | American Health Packaging | 2026-03-03 | HUMAN PRESCRIPTION DRUG LABEL | 3 |