FdaApplication
BLA 103937
Identifiers
- fda_app_no: BLA103937
Properties
| Property | Value |
|---|---|
| applicant_name | Sanofi Vaccines Canada Ltd. |
| application_type | BLA |
| approval_date | 2000-02-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BOTULISM ANTITOXIN BIVALENT (EQUINE) TYPES A AND B. | — | 5000IU | Injection |
1 product