Source: European Medicines Agency (EU) Revision Year: 2019 Publisher: PharmaSwiss Česká republika s.r.o., Jankovcova 1569/2c, 170 00 Praha 7, Czech Republic
Macugen 0.3 mg solution for injection.
Pharmaceutical Form |
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Solution for injection (injection). The solution is clear and colourless. |
One pre-filled syringe provides a usable amount to deliver a single dose of 90 microlitres containing pegaptanib sodium, corresponding to 0.3 mg of the free acid form of the oligonucleotide.
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Pegaptanib |
Pegaptanib is a pegylated modified oligonucleotide that binds with high specificity and affinity to extracellular Vascular Endothelial Growth Factor (VEGF165) inhibiting its activity. VEGF is a secreted protein that induces angiogenesis, vascular permeability and inflammation, all of which are thought to contribute to the progression of the neovascular (wet) form of AMD. |
List of Excipients |
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Sodium chloride |
Each pack contains a pouch in a carton containing a 1 ml pre-filled syringe, Type 1 glass, sealed with an elastomeric (brombutyl rubber) plunger stopper and a pre-attached plunger rod, held by a plastic clip. The syringe has a pre-attached polycarbonate plastic luer lock adaptor and the tip is sealed with an elastomeric (bromobutyl/synthetic isoprene) tip cap.
Each pre-filled syringe contains approximately 0.25-0.27 ml of solution.
Each carton contains one pre-filled syringe in a pouch (single dose pack).
The pack is supplied without a needle.
PharmaSwiss Česká republika s.r.o., Jankovcova 1569/2c, 170 00 Praha 7, Czech Republic
EU/1/05/325/002
Date of first authorisation: 31/01/2006
Date of latest renewal: 19/11/2015
Drug | Countries | |
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MACUGEN | Lithuania, Romania, United States |
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