Midazolam Hydrochloride Injection, Solution
Product Images NDC 23155-600

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Midazolam Hydrochloride (NDC 23155-600). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc., 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

Midazolam Spl Carton Label

Midazolam injection, USP 2 mg/2 mL (1 mg/mL) solution for intramuscular or intravenous use, packaged in 25 single-dose vials of 2 mL each. The label is from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. and includes storage instructions, product composition, and distributor contact information.*

FDA Label Image

Midazolam Spl Fig 1

A line graph showing the pH dependence of the open-ring form of Midazolam hydrochloride in water, with the percentage of open-ring form plotted on the y-axis and pH values on the x-axis. The graph illustrates a decrease in the percentage of open-ring form as pH increases from 2.5 to 5.5.*

FDA Label Image

Midazolam Spl Structure 1

Chemical structure diagram of Midazolam hydrochloride illustrating the molecular framework and arrangement of atoms including nitrogen, chlorine, fluorine, and hydrogen atoms in the compound.*

FDA Label Image

Midazolam Spl Structure 2

Chemical structure diagram showing Midazolam and its open-ring form with detailed molecular connectivity including chlorine, fluorine, and nitrogen atoms.*

FDA Label Image

Midazolam Spl Vial Label

Midazolam hydrochloride Injection, USP 2 mg/2 mL (1 mg/mL) solution label for a 2 mL single-dose vial. The label indicates use for intramuscular or intravenous injection, is sterile, and is distributed by Avet Pharmaceuticals Inc., East Brunswick, NJ. Additional markings include the NDC 23155-600-31, barcode, lot number, expiration date, and manufacturing information noting the product is made in India with a revision date of 02/2020.*

* 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.