| Product NDC: | 49281-915 |
| Proprietary Name: | YF-VAX |
| Non Proprietary Name: | YELLOW FEVER VIRUS LIVE ANTIGEN, A |
| Active Ingredient(s): | & nbsp; YELLOW FEVER VIRUS LIVE ANTIGEN, A |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49281-915 |
| Labeler Name: | Sanofi Pasteur Inc. |
| Product Type: | VACCINE |
| FDA Application Number: | BLA103915 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19530522 |
| Package NDC: | 49281-915-05 |
| Package Description: | 1 KIT in 1 PACKAGE (49281-915-05) * 2.5 mL in 1 VIAL, MULTI-DOSE * 3 mL in 1 VIAL, MULTI-DOSE (49281-912-03) |
| NDC Code | 49281-915-05 |
| Proprietary Name | YF-VAX |
| Package Description | 1 KIT in 1 PACKAGE (49281-915-05) * 2.5 mL in 1 VIAL, MULTI-DOSE * 3 mL in 1 VIAL, MULTI-DOSE (49281-912-03) |
| Product NDC | 49281-915 |
| Product Type Name | VACCINE |
| Non Proprietary Name | YELLOW FEVER VIRUS LIVE ANTIGEN, A |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19530522 |
| Marketing Category Name | BLA |
| Labeler Name | Sanofi Pasteur Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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