Midazolam Hydrochloride
Product Images NDC 55648-765

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.

FDA Label Image

Structure1 (Midazolaminjpf M Figure 01)

Chemical structure of Midazolam hydrochloride, showing its fused ring system with a chlorine substituent and a fluorine atom, along with the hydrochloride (HCl) salt component indicated.*

FDA Label Image

Structure2 (Midazolaminjpf M Figure 02)

Chemical structure diagram showing the equilibrium between Midazolam and its open-ring form. The image depicts the molecular structures of Midazolam and its open-ring form, highlighting their chemical composition and arrangement.*

FDA Label Image

Chart (Midazolaminjpf M Figure 03)

A line graph titled 'pH Dependence of Open-ring Form in Water' showing the percentage of open-ring form plotted against pH values ranging from 2.5 to 5.5. The graph indicates a decrease in the percentage of open-ring form as the pH increases, starting above 50% at pH 2.5 and approaching zero near pH 5.5.*

FDA Label Image

Label (Midazolaminjpf M Figure 04)

Label for Midazolam hydrochloride Injection, USP, 2 mg/2 mL (1 mg/mL) single dose vial by Wockhardt Limited. It is preservative-free, for intramuscular (I.M.) or intravenous (I.V.) use only, and distributed by Wockhardt USA LLC. The label includes barcode, lot, and expiration fields.*

FDA Label Image

Label (Midazolaminjpf M Figure 05)

Midazolam HCl Injection, USP 10 mg/2 mL (5 mg/mL) single dose vial label from Wockhardt Limited. The label states preservative-free, for intramuscular (I.M.) or intravenous (I.V.) use, and includes manufacturer and distributor information. NDC 64679-765-06 is visible along with lot and expiration date areas.*

* 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.