Figure 1 (Praluent 01)
Praluent
Product Images NDC 0024-5904
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 37 technical images submitted to the FDA as part of the official labeling for Praluent (NDC 0024-5904). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Sanofi-aventis U.s. Llc, 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 2 (Praluent 02)
The text describes a table representing data related to the LS mean percent change from the baseline for LDL-C at different time points over 52 weeks for a treatment labeled PRALUENT (N) compared to a placebo treatment. The data shows a considerable decrease in LDL-C levels for the PRALUENT (N) treatment compared to the placebo treatment over the course of 52 weeks.*
Figure 3 (Praluent 03)
This appears to be a graph or chart showing the mean percent change of LDL-C before and after a treatment using a drug called PRALUENT compared to placebo. The graph shows that PRALUENT resulted in a decrease in LDL-C levels compared to placebo at various time points over a period of 52 weeks.*
Figure 4 (Praluent 03a)
This text appears to be a graph or chart that shows the LDL-C LS mean percent change from baseline for three groups over a period of 12 weeks, represented by time points on the x-axis. The groups are labeled as "Placebo," "Praluent75 Q2W," and "Praluent 300 Q4W," and have 157, 78, and 312 subjects, respectively. Without a visual, it is difficult to provide further details.*
Figure 5 (Praluent 03b)
This is a table showing the LDL-C LS Mean Percent Change from Baseline over weeks 4, 8, and 12 for a study comparing PRALUENT 150 mg Q2W (N=45) to a placebo (N=24). The results indicate a -70% reduction in LDL-C for the PRALUENT group compared to the baseline.*
Figure (Praluent 04)
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Figure B (Praluent 24)
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Figure (Praluent 27)
This is a simple instruction to be followed in a situation where a button has been pressed and needs to be released. The instruction is to release the button immediately.*
Figure (Praluent 28)
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Figure (Praluent 31)
Principal Display Panel (75 mg/mL Pen Carton)
Not available. The given text contains mostly symbols, numerals, and some alphabets that are not intelligible.*
Principal Display Panel (150 mg/mL Pen Carton)
Not available. The text contains some words, but they do not make any sense and seem to be randomly arranged.*
Principal Display Panel (75 mg/mL Syringe Carton)
This is a description of Praluent, a medication used as an injection for subcutaneous administration only. It is available in a pre-filled syringe that contains 75mg/mL of the active ingredient alirocumab. The manufacturer of Praluent is Regeneron Sanofi. There is some blurry text at the end that is not readable.*
Principal Display Panel (150 mg/mL Syringe Carton)
The text is a product label of Praluent™ (alirocumab), an injection, containing 150mg/mL of the medication. It recommends the medication for subcutaneous infection only, meant for single-dose use. The label contains information about the manufacturer, dosage, date of infection, and usage instructions.*
* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.
