Bat Purple Book BLA 125462
- BLA number
- 125462
- Proprietary names
- Bat
- Proper names
- Botulism Antitoxin Heptavalent (A, B, C, D, E, F, G) - (Equine)
- Applicant
- Emergent BioSolutions Canada Inc.
- Center
- CBER
- First observed release
- 2020-08-01
- 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 | Bat | Botulism Antitoxin Heptavalent (A, B, C, D, E, F, G) - (Equine) | 351(a) | >4500U | Solution | Intravenous | Single-Dose Vial | Rx | Licensed | 2013-03-22 | |
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 |
|---|
| 2021-09-01 | U | 001 | Bat | 351(a) | Rx | Emergent BioSolutions Canada Inc. |
| 2021-05-01 | U | 001 | Bat | 351(a) | Rx | Emergent BioSolutions Canada Inc. |
| 2020-08-01 | R | 001 | Bat | 351(a) | Rx | Emergent BioSolutions Canada Inc. |
Observed Product State History#
Release, Product, Name table| Release | Product | Name | License type | Marketing | Licensure | Approval |
|---|
| 2020-08-01 | 001 | Bat | 351(a) | Rx | Licensed | 2013-03-22 |