| Product NDC: | 49281-250 |
| Proprietary Name: | IMOVAX RABIES |
| Non Proprietary Name: | RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER |
| Active Ingredient(s): | & nbsp; RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49281-250 |
| Labeler Name: | Sanofi Pasteur Inc. |
| Product Type: | VACCINE |
| FDA Application Number: | BLA103931 |
| Marketing Category: | BLA |
| Start Marketing Date: | 19800609 |
| Package NDC: | 49281-250-51 |
| Package Description: | 1 KIT in 1 CARTON (49281-250-51) * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 SYRINGE (49281-249-01) |
| NDC Code | 49281-250-51 |
| Proprietary Name | IMOVAX RABIES |
| Package Description | 1 KIT in 1 CARTON (49281-250-51) * 1 mL in 1 VIAL, SINGLE-USE * 1 mL in 1 SYRINGE (49281-249-01) |
| Product NDC | 49281-250 |
| Product Type Name | VACCINE |
| Non Proprietary Name | RABIES VIRUS STRAIN PM-1503-3M ANTIGEN (PROPIOLACTONE INACTIVATED) and WATER |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19800609 |
| Marketing Category Name | BLA |
| Labeler Name | Sanofi Pasteur Inc. |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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