Figure (Dupixent 01)
The text provided seems to show a graph. Unfortunately, the graph cannot be interpreted with the information solely provided.*
Dupixent Injection, Solution
Product Images NDC 0024-5915
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 100 technical images submitted to the FDA as part of the official labeling for Dupixent (NDC 0024-5915). 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 (Dupixent 02)
This is a graph showing the proportion of subjects (%) who received either DUPIXENT 300mg Q2W or a placebo over a period of 16 weeks. The proportion of subjects who received DUPIXENT was 36% while the proportion who received a placebo was 5%.*
Figure (Dupixent 03)
This is a chart presenting the proportion of subjects in a study. The study compares the efficacy of Dupilumab (at doses of 200mg or 300mg every two weeks) to a placebo. The chart shows that after 16 weeks, 36.6% of subjects on Dupilumab experienced a positive outcome.*
Figure (Dupixent 04)
Figure (Dupixent 05)
This appears to be a table showing rates and ratios for a drug called Dupixent compared to a placebo. The table includes information on different dosages and categories. However, without additional context or headings, it is difficult to provide a more detailed description of the data presented.*
Figure (Dupixent 06)
This is a table presenting the baseline FeNO group (ppb) and rate ratio for DUPIXENT compared to a Placebo. The values in the table are not interpretable and require further context and information to be understood.*
Figure (Dupixent 07)
This appears to be a clinical trial report for a medication called DUPIXENT. The trial involved 277 participants taking a dosage of 300mg every two weeks, 264 participants taking a dosage of 200mg every two weeks, and a placebo group consisting of 142 participants. The report includes a graph showing the efficacy of the medication over time, with measurements taken at various weeks.*
Figure (Dupixent 08)
This is a table presenting data from a clinical trial that compared the efficacy of Dupixent (at doses of 200mg Q2W and 300mg Q2W) versus placebo. The numbers in the column indicate the sample size for each group, and the values in the last column represent the mean difference (LS) between Dupixent and the placebo group. The numbers in parenthesis indicate the 95% confidence interval for the mean difference. The table suggests that both doses of Dupixent were more effective than the placebo. However, further information on the nature of the trial and study design is required for a more accurate interpretation.*
Figure (Dupixent 09)
This text is a summary table of a clinical trial that compares the effect of two doses of DUPIXENT and placebo on Baseline FeNO levels in a group of subjects. The results indicate that overall, DUPIXENT is better than the placebo in reducing FeNO levels with statistically significant differences between the LS mean difference of DUPIXENT and the placebo for both doses tested. The LS mean difference between the DUPIXENT doses is not shown.*
Figure (Dupixent 10)
This is a study comparing the effectiveness of a drug called Dupixent at two different doses (300 mg and 200 mg) every two weeks vs placebo in a sample of 733 individuals. The text includes data on the number of participants in each group over the course of 52 weeks, as well as the mean change in an unspecified outcome variable measured at various time points.*
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The text describes the contents of a pre-filed syringe of DUPIXENT, which includes one alcohol wipe, one cotton ball or gauze, and a sharps disposal container. DUPIXENT is a medication used to treat certain inflammatory conditions like eczema and asthma.*
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Figure (Dupixent 11)
This appears to be a chart or graph showing change in ppFEV1 (a measure of lung function) over time in weeks for a group of 175 people taking Dupixent compared to a group of 84 people taking a placebo. The indicated LS (least squares) mean change is -8 for the Dupixent group. The SE (standard error) values are given as 12.43 at week 0 and 4.08 at week 52.*
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Dupixent 11a
This data appears to be results from a study comparing the medication Dupixent 300 mg to a placebo taken every two weeks. The chart shows the LS Mean Change +/-SE (standard error) over weeks 8 through 40, with possibly some measurements at 0.5, 5.4, and -1.04. It is not clear what the units of measurement or the specific condition being treated are.*
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This text shows the mean change of DUPIXENT (a medication) compared to a placebo every two weeks over a period of 48 weeks, based on a sample size of 143 and 133 respectively. The mean change is presented in percentages at different time intervals (weeks).*
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This is a clinical trial report comparing the effect of Dupixent 300 mg Q2W with placebo Q2W on an unknown health condition. The report shows the number of participants in each group (438 in the Dupixent group and 286 in the placebo group) along with their status at different time points (4, 8, 12, 16, 20, 28, 32, 36, 40, 44, 48, 52 weeks). The report also shows the number of participants at risk at each time point.*
Figure (Dupixent 12)
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A medication named Dupixent with the NDC code 0024-5914.01 is described. It is an injection given subcutaneously (under the skin). Each pre-filled syringe contains 300mg/2mL of dupilumab. The medication should be stored at a temperature of 2°C to 8°C and must be protected from light. The product must not be frozen. The medication is manufactured by Sanofi Genzyme and Regeneron. Detailed instructions regarding dosage and administration can be found in the package insert.*
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This is a description of a drug called Dupixent, which is administered through subcutaneous injection. The drug comes in a prefilled syringe and each syringe delivers a 200mg dose. The drug must be stored in a refrigerator at a temperature of 36-46°F and protected from light. It should not be used after 14 days or if it has been exposed to direct sunlight. The package insert should be reviewed for dosage and administration information. These details are important to ensure proper use and effectiveness of the drug.*
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This is a product information label for Dupixent, an injection medication used to treat certain inflammatory conditions such as eczema and asthma. It comes in a single-dose pre-filled pen containing 300mg/2mL of dupilumab, to be administered subcutaneously. The pen also includes several other ingredients, including L-arginine hydrochloride and sucrose. The package includes instructions for use and dosage information. It is important to store the medication at room temperature and avoid exposure to sunlight for up to 14 days. NDC code: 0024-5915-02.*
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This is packaging information for Dupixent, a medication that is stored refrigerated and kept away from heat sources. It is administered via injection and comes in a single-dose, pre-filled pen. The packaging gives instructions for dosing and administration, and includes a warning to keep the medication out of reach of children. The text also includes various identification codes for the product.*
Figure (Dupixent 13)
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This is a description of DUPiXENT, a medication that comes in single-dose pre-filled syringes for injection. Each syringe contains 100 mg of dupilumab, which is intended to be kept at room temperature for up to 14 days. The medication should not be exposed to temperatures above 77°F (25°C) and should be discarded after use. The recommended dosage and administration instructions can be found in the package insert, and more information about DUPiXENT can be found at DUPiXENTinfo.com.*
Figure (Dupixent 14)
Figure (Dupixent 15)
This is a pack of DUPIXENT pre-filled syringes along with an alcohol wipe, a cotton ball or gauze and a sharps disposal container for safe disposal of used syringes.*
Figure (Dupixent 16)
Figure (Dupixent 17)
Figure (Dupixent 18)
Principal Display Panel (300 mg/2 mL Syringe Carton)
This text is not comprehensive enough to provide a useful description.*
Principal Display Panel (300 mg/2 mL Syringe Carton)
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This is a description of the contents of a DUPIXENT pre-filled syringe package. It includes one alcohol wipe and a sharps disposal container.*
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This description is for a product or an element in a user interface that is called "Viewing Window". No further information is provided.*
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This is a description of a product for maintaining medical hygiene. The product is a container for disposing of used syringes and other sharps.*
Dupixent 42
This text appears to be describing an injection process. It shows "Before Injection" and "After Injection" sections with some related details, such as the color of the window changing from yellow to indicate that the injection is complete. Additionally, there are descriptions of various items including a green cap, medicine label, and yellow needle cover. The text does not provide enough information to determine what type of injection, medication, or medical procedure is being performed.*
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The text describes the contents of a package of DUPIXENT pre-filled pen. It includes a cotton ball or gauze, an alcohol wipe and a sharps disposal container. However, these items are not included in the carton.*
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* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
