Synagis - 60574-4113-1 - (palivizumab)

Alphabetical Index


Drug Information of Synagis

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)

Labeler Information of Synagis

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 Information of Synagis

Package NDC: 60574-4113-1
Package Description: 1 mL in 1 VIAL, SINGLE-DOSE (60574-4113-1)

NDC Information of Synagis

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]

Complete Information of Synagis


General Information