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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tranexamic Acid
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRANEXAMIC ACID | 650 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6T84R30KC1 |
| Rxcui | 883826 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60687-750-11 | Tranexamic Acid | 1 in 1 BLISTER PACK | TABLET | 1 | | 3 |
| 60687-750-21 | Tranexamic Acid | 30 in 1 CARTON | TABLET | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60687-750 | TRANEXAMIC ACID TABLET [AMERICAN HEALTH PACKAGING] | 2 | Current NDC, 2 package rows | 20241030_cbc6f5b3-927e-4a94-8836-dbcd47ef97a8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60687-750-11 | 60687075011 | 1 in 1 BLISTER PACK | | | | | Historical |
| 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 | Current |