Active Ingredient(s): Palivizumab
FDA Approved: * June 19, 1998
Pharm Company: * MEDIMMUNE
Category: Vaccination

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Synagis Overview

Palivizumab, sold under the brand name Synagis, is a monoclonal antibody produced by recombinant DNA technology used to prevent severe disease caused by respiratory syncytial virus (RSV) infections.[2][3] It is recommended for infants that are high-risk because of prematurity or other medical problems such as congenital heart disease.[2][3] The most common side effects include fever and rash.[2][3]...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source:

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Possible Dosages for this and Related Drugs:

  • Injection: 100mg, 100mg/ml, 50mg, 50mg/ml
  • Vial: 100mg/vial, 50mg/vial
Note: Above list includes dosages for all drugs with the same combination of active ingredients.

NDC Database Records for Synagis: (4 results)

Sorted by National Drug Code
  • 60574-4113 Synagis 100 mg/ml Intramuscular Injection, Solution by Medimmune, LLC
  • 60574-4114 Synagis 50 mg/.5ml Intramuscular Injection, Solution by Medimmune, LLC
  • 66658-230 Synagis 50 mg/.5ml Intramuscular Injection, Solution by Swedish Orphan Biovitrum Ab (Publ)
  • 66658-231 Synagis 100 mg/ml Intramuscular Injection, Solution by Swedish Orphan Biovitrum Ab (Publ)

Other drugs which contain Palivizumab or a similar ingredient: (1 result)

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