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. |
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Strength Number | |
Strength Unit | |
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