Synagis - 60574-4114-1 - (palivizumab)

Alphabetical Index


Drug Information of Synagis

Product NDC: 60574-4114
Proprietary Name: Synagis
Non Proprietary Name: palivizumab
Active Ingredient(s): 50    mg/.5mL & nbsp;   palivizumab
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Synagis

Product NDC: 60574-4114
Labeler Name: MedImmune, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103770
Marketing Category: BLA
Start Marketing Date: 19991209

Package Information of Synagis

Package NDC: 60574-4114-1
Package Description: .5 mL in 1 VIAL, SINGLE-DOSE (60574-4114-1)

NDC Information of Synagis

NDC Code 60574-4114-1
Proprietary Name Synagis
Package Description .5 mL in 1 VIAL, SINGLE-DOSE (60574-4114-1)
Product NDC 60574-4114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name palivizumab
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR
Start Marketing Date 19991209
Marketing Category Name BLA
Labeler Name MedImmune, LLC
Substance Name PALIVIZUMAB
Strength Number 50
Strength Unit mg/.5mL
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