Botulism Antitoxin Bivalent (Equine) Types A and B. Purple Book BLA 103937
- BLA number
- 103937
- Proper names
- Botulism Antitoxin Bivalent (Equine) Types A and B.
- Applicant
- Sanofi Vaccines Canada Ltd.
- Center
- CBER
- First observed release
- 2022-05-01
- 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 | | Botulism Antitoxin Bivalent (Equine) Types A and B. | 351(a) | 5000IU | Injection | Intravenous | Vial | Rx | Voluntarily Revoked | 2000-02-24 | |
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 |
|---|
| 2026-05-01 | U | 001 | Botulism Antitoxin Bivalent (Equine) Types A and B. | 351(a) | Rx | Sanofi Vaccines Canada Ltd. |
| 2022-05-01 | N | 001 | Botulism Antitoxin Bivalent (Equine) Types A and B. | 351(a) | Rx | Sanofi Pasteur Limited |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2022-05-01 | 001 | Botulism Antitoxin Bivalent (Equine) Types A and B. | 351(a) | Rx | Voluntarily Revoked | 2000-02-24 |