Structure1 (Midazolaminjpf M Figure 01)
Midazolam Hydrochloride
Product Images NDC 55648-765
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Midazolam Hydrochloride (NDC 55648-765). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Wockhardt Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Structure2 (Midazolaminjpf M Figure 02)
Chart (Midazolaminjpf M Figure 03)
The text describes a graph that shows the dependence of the open-ring form in water at different pH levels. The x-axis is labeled as pH values ranging from 2 to 5, while the y-axis is labeled as the percentage of the open-ring form, which ranges from 0% to 80%.*
Label (Midazolaminjpf M Figure 04)
This is a label of a drug called Midazolam HCI Injection, USP manufactured by Wockhardt Limited in Aurangabad, Maharashtra, India. The size of the dose is 2mg/2mL and it is distributed by NDC. The label includes a disclaimer to discard any unused portion of the medicine. There is some text that is not readable, possibly due to errors.*
Label (Midazolaminjpf M Figure 05)
This is a medication for injection called Midazolam HCI manufactured by Wockhardt Limited and distributed by Wockhardt USA LLC. It comes in a 10 mg/2 mL dosage and is prescription-only. The packaging indicates that any unused portion should be discarded. It also appears to be preservative-free. There is additional information regarding the manufacturer, including an address in India and a distribution center in New Jersey. The meaning of the final line of text is unclear.*
* 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.
