Midazolam In 0.8% Sodium Chloride Injection, Solution
Product Images NDC 0264-8002

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This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Midazolam In 0.8% Sodium Chloride (NDC 0264-8002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by B. Braun Medical 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

Structural Formula (Midazolam In Sodium Chloride Injection 1)

FDA Label Image

Schedule Iv Controlled Substance Symbol (Midazolam In Sodium Chloride Injection 2)

FDA Label Image

Dm8005 Container Label (Midazolam In Sodium Chloride Injection 3)

Dm8005 Container Label (Midazolam In Sodium Chloride Injection 3)
This text is about a 50 mL single-dose container of Midazolam solution in 0.8% Sodium Chloride Injection for intravenous use only. The solution contains 1 mg of Midazolam per mL. It is essential not to add supplementary medication, use in series connections, or use if leaks are present. The solution should be clear before use. It needs to be stored at 20°C to 25°C and protected from freezing and light. The solution is sterile, nonpyrogenic, preservative-free, and isotonic. Unused portions should be discarded, and the container is not made with natural rubber.*
FDA Label Image

Schedule Iv Controlled Substance Symbol (Midazolam In Sodium Chloride Injection 4)

FDA Label Image

Dm8002 Container Label (Midazolam In Sodium Chloride Injection 5)

Dm8002 Container Label (Midazolam In Sodium Chloride Injection 5)
This is a description of a medication called Midazolam, which is provided in a 100 mL single-dose container at a concentration of 100 mg per 100 mL (1 mg per mL) in 0.8% Sodium Chloride Injection for intravenous use only. The text also mentions not to add additional medication or use in series connections. It is essential to check for leaks, and if any are found, the container should be discarded. The solution should be clear for use. Each mL contains 1 mg of Midazolam, 8 mg of Sodium Chloride in Water for Injection, and may contain Hydrochloric Acid or Sodium Hydroxide to adjust the pH. The medication is sterile, nonpyrogenic, preservative-free, and isotonic. The dosage and administration instructions are detailed in the package insert. The medication should be stored at 20°C to 25°C with excursions between 15°C to 30°C, protected from freezing and light. Additionally, it is mentioned that the product is not made with latex, PVC, or DEHP.*
FDA Label Image

Schedule Iv Controlled Substance Symbol (Midazolam In Sodium Chloride Injection 6)

FDA Label Image

Dm8005 Overwrap (Midazolam In Sodium Chloride Injection 7)

Dm8005 Overwrap (Midazolam In Sodium Chloride Injection 7)
This is a description of a pharmaceutical product in a 50 mL single-dose container for intravenous use only, containing 50 mg per 50 mL (1 mg per mL) of Midazolam injection solution. The container should be checked for leaks before usage. Each mL of the solution contains 1 mg Midazolam, 8 mg Sodium Chloride, and may contain Hydrochloric Acid and/or Sodium Hydroxide to adjust the pH. The dosage and administration instructions are provided in the package insert. It is recommended to store the product in the original overwrap protected from light until ready to use. The product is preservative-free and should be discarded if unused. Not-made with natural rubber latex, PVC, or DEHP.*
FDA Label Image

Schedule Iv Controlled Substance Symbol (Midazolam In Sodium Chloride Injection 8)

FDA Label Image

Dm8002 Overwrap (Midazolam In Sodium Chloride Injection 9)

Dm8002 Overwrap (Midazolam In Sodium Chloride Injection 9)
This is a description for an intravenous solution of Midazolam, with a concentration of 1 mg per mL. It comes in a single-dose container and should only be used for intravenous administration. The solution also contains Sodium Chloride and is stored at room temperature, protected from light. The packaging has instructions on how to open and check for leaks before use. The manufacturer is B. Braun Medical Inc. and it is prepared in Canada. For more detailed prescribing information, the package insert should be consulted.*

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