LUCENTIS (ranibizumab injection) Intravitreal Injection. Initial U.S. Approval: 2006

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LUCENTIS (ranibizumab injection) Intravitreal Injection. Initial U.S. Approval: 2006

INDICATIONS AND USAGE
LUCENTIS, a vascular endothelial growth factor (VEGF) inhibitor, is indicated for the treatment of patients with:
• Neovascular (Wet) Age-Related Macular Degeneration (AMD)
• Macular Edema Following Retinal Vein Occlusion (RVO)
• Diabetic Macular Edema (DME)
DOSAGE FORMS & STRENGTHS
Single-use glass vial designed to provide 0.05 mL for intravitreal injections:
• 10 mg/mL solution (LUCENTIS 0.5 mg)
• 6 mg/mL solution (LUCENTIS 0.3 mg)
Manufactured By: Genentech
Prescribing Information URL: Click Here

Access to LUCENTIS (ranibizumab injection) Intravitreal Injection: Anticancer drugs available upon request. To get best price please share your mobile number to receive quotes from Medvitaz Pharma Solutions.

Ranibizumab (trade name Lucentis among others) is a monoclonal antibody fragment (Fab) created from the same parent mouse antibody as bevacizumab. It is an anti-angiogenic that has been approved to treat the "wet" type of age-related macular degeneration (AMD, also ARMD), diabetic retinopathy, and macular edema due to branch retinal vein occlusion or central retinal vein occlusion.
Ranibizumab was developed by Genentech and marketed by them in the United States, and elsewhere by Novartis, under the brand name Lucentis.

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