Veopoz Purple Book BLA 761339
- BLA number
- 761339
- Proprietary names
- Veopoz
- Proper names
- pozelimab-bbfg
- Applicant
- Regeneron Pharmaceuticals, Inc.
- Center
- CDER
- First observed release
- 2023-08-01
- Latest observed release
- 2026-06-01
- Newest archive release
- 2026-06-01
- FDA patent list
- No patents listed in the captured FDA patent list; source updated 2025-06-11
- Coverage
- Present in newest release
Latest Known Product Presentations#
Product, Proprietary name, Proper name table| Product | Proprietary name | Proper name | License type | Strength | Dosage form | Route | Presentation | Marketing | Licensure | Approval | Patent list provided |
|---|
| 001 | Veopoz | pozelimab-bbfg | 351(a) | 400MG/2ML (200MG/ML) | Injection | Intravenous, Subcutaneous | Single-Dose Vial | Rx | Licensed | 2023-08-18 | |
Published Patent List#
No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.
Official Monthly Change Events#
Release, Event, Product table| Release | Event | Product | Name | License type | Status | Applicant |
|---|
| 2023-11-01 | U | 001 | Veopoz | 351(a) | Rx | Regeneron Pharmaceuticals, Inc. |
| 2023-09-01 | N | 001 | Veopoz | 351(a) | Rx | Regeneron Pharmaceuticals, Inc. |
| 2023-08-01 | N | 001 | Veopoz | 351(a) | Rx | Regeneron Pharmaceuticals, Inc. |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2023-08-01 | 001 | Veopoz | 351(a) | Rx | Licensed | 2023-08-18 |