ELIQUIS
- Product NDC
- 67296-1673
- 11-digit product format
- 672961673
- Labeler code
- 67296
- Product ID
- 67296-1673_b95b2fc2-aca9-e8e8-e053-2a95a90a0e2a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apixaban
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- NDA202155
- Marketing category
- NDA
- Marketing start
- 2019-01-01
- Marketing end
- 0000-00-00
- Substance
- APIXABAN
- Active strength
- 5 mg/1
- Pharmacologic classes
- Factor Xa Inhibitor [EPC],Factor Xa Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1673-1 | ELIQUIS | 12 in 1 BOTTLE | TABLET, FILM COATED | 12 | | 9 |
| 67296-1673-7 | ELIQUIS | 14 in 1 BOTTLE | TABLET, FILM COATED | 14 | | 9 |
| 67296-1673-8 | ELIQUIS | 28 in 1 BOTTLE | TABLET, FILM COATED | 28 | | 9 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1673 | ELIQUIS (APIXABAN) TABLET, FILM COATED [REDPHARM DRUG, INC.] | 9 | Legacy NDC, 3 package rows | 20240805_8917e527-990a-17c0-e053-2a95a90a4631.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1673-1 | 67296167301 | 12 TABLET, FILM COATED in 1 BOTTLE (67296-1673-1) | 2019-01-01 | 0000-00-00 | No | No | Current |
| 67296-1673-7 | 67296167307 | 14 TABLET, FILM COATED in 1 BOTTLE (67296-1673-7) | 2021-01-01 | 0000-00-00 | No | No | Current |
| 67296-1673-8 | 67296167308 | 28 TABLET, FILM COATED in 1 BOTTLE (67296-1673-8) | 2019-01-01 | 0000-00-00 | No | No | Current |