Vecuronium Bromide
Product Images NDC 47335-932

3 FDA label images from Sun Pharmaceutical Industries, Inc. · 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 47335-932). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Vecuronium-carton-10mg (Vecuronium Carton 10mg)

Vecuronium-carton-10mg (Vecuronium Carton 10mg)
The image depicts a packaging label for Vecuronium Bromide for Injection, 10 mg (1 mg/mL when reconstituted to 10 mL), a lyophilized powder provided in 10 x 10 mg vials. The label emphasizes it is for intravenous single use only and is labeled Rx only. The product is manufactured by Sun Pharmaceutical Industries Ltd. and distributed by Sun Pharmaceutical Industries, Inc.*
FDA Label Image

Vecuronium-carton-20mg (Vecuronium Carton 20mg)

Vecuronium-carton-20mg (Vecuronium Carton 20mg)
Label for Vecuronium Bromide for Injection 20 mg (1 mg/mL when reconstituted to 20 mL) lyophilized powder by Sun Pharmaceutical Industries, Inc. The label states it is for IV single use only and includes packaging for 10 vials of 20 mg each. The label includes warnings about paralysis and respiratory arrest and storage instructions.*
FDA Label Image

Vecuronium-chem-str (Vecuronium Chem Str)

Vecuronium-chem-str (Vecuronium Chem Str)
Chemical structure of vecuronium bromide depicted as a detailed molecular diagram showing the arrangement of atoms and bonds, including rings and functional groups, with the bromide ion indicated separately.*

* 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.