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

This is a product description for Midazolam Injection, USP, a medication to be used for intramuscular and intravenous use only. It comes in a package of 25 single-dose vials containing 2 mg/2 mL (1mg/mL) of midazolam hydrochloride, adjusted with hydrochloric acid and sodium hydroside to a pH level of 2.0 to 3.5. Each mL contains 1 mg of the active ingredient and is combined with 0.8% sodium chloride and 0.01% edetate disodium. The medication needs to be stored at a controlled room temperature, and any unused portions must be discarded. The product is distributed by Avet Pharma.*

FDA Label Image

Midazolam Spl Fig 1

FDA Label Image

Midazolam Spl Structure 1

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Midazolam Spl Structure 2

FDA Label Image

Midazolam Spl Vial Label

This is a description of a medication with the NDC number 23155-600-31, called Midazolam. It is an injection, with a strength of 2 mg/2 mL, and a concentration of 1 mg/mL. This medication is made in India and is sterile. It is intended for use in either the LM or LV. The lot number is unvamish area, and the expiration date is listed as 13x10mm.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.