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Chemical structure of sumatriptan succinate, showing the molecular arrangement of its atoms and bonds relevant to this active ingredient.*
Sumatriptan Succinate Injection
Product Images NDC 63323-273
6 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Sumatriptan Succinate (NDC 63323-273). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Fresenius Kabi Usa, 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
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A line graph comparing the estimated percentage of subjects experiencing relief over time (in minutes) for Sumatriptan Succinate injection 6 mg/0.5 mL subcutaneous versus placebo. The graph shows higher relief percentages in the Sumatriptan group over a 25-minute period.*
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Label for Sumatriptan Injection, USP 6 mg/0.5 mL by Fresenius Kabi USA, LLC. The packaging indicates a 0.5 mL single-dose vial for subcutaneous injection, marked Rx only. It includes the NDC 63323-273-01 and notes to discard any unused portion.*
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Label for Sumatriptan Injection, USP 6 mg per 0.5 mL, a subcutaneous injection by Fresenius Kabi USA, LLC. It is a 0.5 mL single-dose vial. The label includes dosage strength, NDC 63323-273-01, storage instructions to keep between 2° to 25°C, and a note that the container closure is not made with natural rubber latex. The label also states it is for subcutaneous injection only and provides the manufacturer's website.*
* 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.
