Rocuronium Bromide Solution
Product Images NDC 71872-7036

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Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Rocuronium Bromide (NDC 71872-7036). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Pdp (7036)

Pdp (7036)
This is a description of Rocuronium Bromide Injection, which is a sterile, non-pyrogenic solution available in a 50 mg/5 mL (10 mg/mL) 5 mL multiple dose vial for intravenous use only. The warning indicates that it may cause respiratory depression, so facilities for artificial respiration must be immediately available. The recommended storage temperature is 2-8°C (38-46°F) and the product should not be frozen. The product must be used within 60 days after removal from refrigeration to room temperature storage conditions (25°C/77°F). This product has been manufactured by X.Gan Pharmaceuticals, Inc. in Germany and is distributed by Medical Purchasing Solutions in Scottdale, AZ.*
FDA Label Image

Structural Formula (Rocuronium Bromide Injection 1)

Structural Formula (Rocuronium Bromide Injection 1)
FDA Label Image

Figure 1 (Rocuronium Bromide Injection 2)

Figure 1 (Rocuronium Bromide Injection 2)
FDA Label Image

Figure 2 (Rocuronium Bromide Injection 3)

Figure 2 (Rocuronium Bromide Injection 3)
FDA Label Image

Figure 3 (Rocuronium Bromide Injection 4)

Figure 3 (Rocuronium Bromide Injection 4)
FDA Label Image

5 mL Vial Label (Rocuronium Bromide Injection 5)

5 mL Vial Label (Rocuronium Bromide Injection 5)

* 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.