Vecuronium Bromide Injection
Product Images NDC 83301-0056

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Vecuronium Bromide (NDC 83301-0056). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mullan Pharmaceutical 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

Chemical Structure (Vecuronium 01)

Chemical Structure (Vecuronium 01)
Chemical structure of Vecuronium Bromide, showing its molecular framework with rings, side chains, and bromide ion representation as part of the compound.*
FDA Label Image

Principal Display Panel (10 mL Vial Carton)

Principal Display Panel (10 mL Vial Carton)
Packaging label for Vecuronium Bromide for Injection 10 mg lyophilized powder, for intravenous use only. The label includes warnings indicating it is a paralyzing agent. It is supplied by Mullan Pharmaceutical Inc. The label notes reconstitution to a concentration of 1 mg/mL in 10 mL. The label also shows storage instructions and manufacturer details, including a barcode and NDC 83301-0056-2.*
FDA Label Image

Principal Display Panel (20 mL Vial Carton)

Principal Display Panel (20 mL Vial Carton)
Label for Vecuronium Bromide for Injection 20 mg lyophilized powder in a carton containing 10 vials of 20 mg each. The label indicates the product is for intravenous use only, supplied by Mullan Pharmaceutical Inc., and includes warnings such as "Paralyzing Agent." The label features dosage concentration details and storage instructions, with the manufacturer listed as Gland Pharma Limited, India.*

* 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.