ELIQUIS
- Product NDC
- 70518-4462
- 11-digit product format
- 705184462
- Labeler code
- 70518
- Product ID
- 70518-4462_3d82588d-1d34-1c57-e063-6294a90af174
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- apixaban
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA202155
- Marketing category
- NDA
- Marketing start
- 2025-08-29
- 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 |
|---|
| 70518-4462-0 | ELIQUIS | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4462-0 | 70518446200 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4462-0) | 2025-08-29 | No | No | Historical |