Lucentis Injection, Solution
Product Images NDC 50242-080
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 25 technical images submitted to the FDA as part of the official labeling for Lucentis (NDC 50242-080). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Genentech, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Figure (Lucentis 02)
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Figure 2 (Lucentis 16)
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Principal Display Panel (0.5 mg Syringe Label)
This is a description of a drug product called Lucentis. It is a sterile, single-use syringe used for intravitreal injection only. The drug is indicated for the treatment of wet age-related macular degeneration (WAMD), macular edema following retinal vein occlusion (RVO), and myopic choroidal neovascularization (mCNV). The syringe contains 0.5mg of ranibizumab. It is important to keep the product refrigerated and protected from light. It is manufactured by Genentech and is identified by the NDC code 50242.080-03.*
Principal Display Panel (0.3 mg Syringe Packet)
This is a description of a medication called Lucentis (ranibizumab injection) that comes in a pre-filled syringe with a 0.3 mg dose. It is used for intravitreal injection only and is indicated for treating diabetic macular edema (DME) and diabetic retinopathy (DR). The medication is sterile, for single use only and should be kept refrigerated, protected from light, and not frozen. The text also includes the National Drug Code (NDC) number and an identification number (10198958).*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.