Vecuronium Bromide Injection, Powder, Lyophilized, For Solution
Product Images NDC 67457-438

3 FDA label images from Mylan Institutional Llc · 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 67457-438). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Structural Formula (Image 01)

Structural Formula (Image 01)
Chemical structure of vecuronium bromide shown as a detailed molecular diagram depicting its carbon rings, functional groups, and bromide ion (Br-). This skeletal formula illustrates the arrangement of atoms and bonds characteristic of this neuromuscular blocking agent.*
FDA Label Image

10 mg Carton (Image 02)

10 mg Carton (Image 02)
Packaging label for Vecuronium Bromide injection, lyophilized powder for solution, 10 mg strength, in single-dose vials. The label indicates it is for intravenous use only and contains 10 vials of 10 mg each. The labeler is Mylan Institutional LLC. The label includes warnings about its paralyzing agent properties and storage instructions.*
FDA Label Image

20 mg Carton (Image 03)

20 mg Carton (Image 03)
Packaging label for Vecuronium Bromide 20 mg injection, lyophilized powder for intravenous use, manufactured by Mylan Institutional LLC. The label indicates single-dose vials with 10 vials of 20 mg each, to be reconstituted to 1 mg/mL in 20 mL. Includes warnings of paralytic effects and storage instructions.*

* 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.