ELIQUIS
- Product NDC
- 50090-6454
- 11-digit product format
- 500906454
- Labeler code
- 50090
- Product ID
- 50090-6454_d32cc824-92b9-4b7e-969f-181b7f5d815d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apixaban
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA202155
- Marketing category
- NDA
- Marketing start
- 2012-12-28
- Substance
- APIXABAN
- Active strength
- 5 mg/1
- Pharmacologic classes
- Factor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ELIQUIS
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| APIXABAN | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 3Z9Y7UWC1J |
| Rxcui | 1364445, 1364447 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6454-0 | ELIQUIS | 60 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6454 | ELIQUIS (APIXABAN) TABLET, FILM COATED [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, 1 package rows | 20230511_2f47aa0e-0235-4220-85dd-dfcb8ad0d009.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6454-0 | 50090645400 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-6454-0) | 2023-04-27 | No | No | Current |