NUWIQ
- Product NDC
- 68982-143
- 11-digit product format
- 689820143
- Labeler code
- 68982
- Product ID
- 68982-143_0868958e-3f70-f70a-5acd-bb3d002fe86f
- Type
- PLASMA DERIVATIVE
- Nonproprietary name
- Antihemophilic Factor (Recombinant)
- Dosage form
- KIT
- Route
- INTRAVENOUS
- Labeler
- Octapharma USA Inc
- Application
- BLA125555
- Marketing category
- BLA
- Marketing start
- 2016-01-01
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- NUWIQ
- Listing expiration
- 2026-12-31
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68982-143-01 | NUWIQ | 1 in 1 CARTON | KIT | 1 | | 16 |
| 68982-144-01 | NUWIQ | 2.5 mL in 1 VIAL | POWDER, FOR SOLUTION | 2.5 mL | 1000 [iU] in 2.5mL | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68982-143 | NUWIQ (ANTIHEMOPHILIC FACTOR (RECOMBINANT)) KIT [OCTAPHARMA USA INC] | 16 | Current NDC, Legacy NDC, 2 package rows | 20250201_d6cb51f8-3acd-412c-93ec-41a8017dff3e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68982-143-01 | 68982014301 | 1 KIT in 1 CARTON (68982-143-01) * 2.5 mL in 1 VIAL (68982-144-01) * 2.5 mL in 1 VIAL (68982-901-01) | 1 kit | 2016-01-01 | 0000-00-00 | No | No | Current |
| 68982-144-01 | 68982014401 | 2.5 mL in 1 VIAL | 2.5 ml | | | | | Historical |