Product NDC: | 60574-4113 |
Proprietary Name: | Synagis |
Non Proprietary Name: | palivizumab |
Active Ingredient(s): | 100 mg/mL & nbsp; palivizumab |
Administration Route(s): | INTRAMUSCULAR |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60574-4113 |
Labeler Name: | MedImmune, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103770 |
Marketing Category: | BLA |
Start Marketing Date: | 19980619 |
Package NDC: | 60574-4113-1 |
Package Description: | 1 mL in 1 VIAL, SINGLE-DOSE (60574-4113-1) |
NDC Code | 60574-4113-1 |
Proprietary Name | Synagis |
Package Description | 1 mL in 1 VIAL, SINGLE-DOSE (60574-4113-1) |
Product NDC | 60574-4113 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | palivizumab |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAMUSCULAR |
Start Marketing Date | 19980619 |
Marketing Category Name | BLA |
Labeler Name | MedImmune, LLC |
Substance Name | PALIVIZUMAB |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Antibodies, Monoclonal [Chemical/Ingredient],Fusion Protein Inhibitors [MoA],Respiratory Syncytial Virus Anti-F Protein Monoclonal Antibody [EPC] |