Tranexamic Acid
- Product NDC
- 71335-1957
- 11-digit product format
- 713351957
- Labeler code
- 71335
- Product ID
- 71335-1957_d7cc42b6-9601-4a5c-ac35-c6d130c1072c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Tranexamic Acid
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA022430
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-03-01
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-1957 | TRANEXAMIC ACID TABLET [BRYANT RANCH PREPACK] | 102 | Legacy NDC | 20230328_0905adcf-2d64-45c9-90d3-ee56e544f155.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1957-1 | 71335195701 | 8 TABLET in 1 BOTTLE (71335-1957-1) | 8 tablet | 2021-10-06 | 0000-00-00 | No | No | Current |
| 71335-1957-2 | 71335195702 | 30 TABLET in 1 BOTTLE (71335-1957-2) | 30 tablet | 2021-10-06 | 0000-00-00 | No | No | Current |