Product NDC: | 49281-190 |
Proprietary Name: | IMOGAM RABIES-HT |
Non Proprietary Name: | HUMAN RABIES VIRUS IMMUNE GLOBULIN |
Active Ingredient(s): | 150 [iU]/mL & nbsp; HUMAN RABIES VIRUS IMMUNE GLOBULIN |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49281-190 |
Labeler Name: | Sanofi Pasteur Inc. |
Product Type: | PLASMA DERIVATIVE |
FDA Application Number: | BLA103932 |
Marketing Category: | BLA |
Start Marketing Date: | 19840427 |
Package NDC: | 49281-190-20 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 CARTON (49281-190-20) > 2 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 49281-190-20 |
Proprietary Name | IMOGAM RABIES-HT |
Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (49281-190-20) > 2 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 49281-190 |
Product Type Name | PLASMA DERIVATIVE |
Non Proprietary Name | HUMAN RABIES VIRUS IMMUNE GLOBULIN |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19840427 |
Marketing Category Name | BLA |
Labeler Name | Sanofi Pasteur Inc. |
Substance Name | HUMAN RABIES VIRUS IMMUNE GLOBULIN |
Strength Number | 150 |
Strength Unit | [iU]/mL |
Pharmaceutical Classes |