CYTOGAM Solution for infusion Ref.[10798] Active ingredients: Cytomegalovirus immunoglobulin

Source: FDA, National Drug Code (US)  Revision Year: 2018 

Product description

CYTOGAM, Cytomegalovirus Immune Globulin Intravenous (Human) (CMV-IGIV), is an immunoglobulin G (IgG) containing a standardized amount of antibody to Cytomegalovirus (CMV). CMV-IGIV is formulated in final vial as a sterile liquid. The globulin is stabilized with 5% sucrose and 1% Albumin (Human). CYTOGAM contains no preservative. The purified immunoglobulin is derived from pooled adult human plasma selected for high titers of antibody for Cytomegalovirus (CMV).1 Source material for fractionation may be obtained from another U.S. licensed manufacturer. Pooled plasma was fractionated by ethanol precipitation of the proteins according to Cohn Methods 6 and 9, modified to yield a product suitable for intravenous administration. A widely utilized solvent-detergent viral inactivation process is also used.2 Certain manufacturing operations may be performed by other firms. Each milliliter contains: 50 ± 10 mg of immunoglobulin, primarily IgG, and trace amounts of IgA and IgM; 50 mg of sucrose; 10 mg of Albumin (Human). The sodium content is 20-30 mEq per liter, i.e., 0.4-0.6 mEq per 20 mL or 1.0-1.5 mEq per 50 mL. The solution should appear colorless and translucent.

How Supplied

CYTOGAM is supplied in a 50 mL single-dose vial (50 mg/mL).

The product presentation includes a package insert and the following component:

Presentation Carton NDC Number Component
2.5 g 44206-532-11 CYTOGAM in a single-use vial [NDC 44206-532-90]

Manufactured by: CSL Behring AG, Bern, Switzerland, US License No. 1766

Distributed by: CSL Behring LLC, Kankakee, IL 60901 USA

Drugs

Drug Countries
CYTOGAM Canada, United States

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