Vecuronium Bromide Injection, Powder, Lyophilized, For Solution
Product Images NDC 51662-1547

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Vecuronium Bromide (NDC 51662-1547). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Labeling (51662 1547 1 Serialized Labeling)

Vecuronium Bromide injection vial labeled for intravenous use, containing 10 mg per vial of lyophilized powder for solution. The vial has a white label with black and pink text, a red cap, and includes the product NDC 05550-235-06. The labeler is HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Boxed Warning (Boxed Warning)

A drug facts or instructions panel stating that the drug should be administered by adequately trained individuals familiar with its actions, characteristics, and hazards. The text advises caution and proper training for administration.*

FDA Label Image

Dosage (Dosage)

Two tables showing infusion rates for vecuronium bromide. The first table relates drug delivery rate (mcg/kg/min) to infusion delivery rate (mL/kg/min) for 0.1 mg/mL and 0.2 mg/mL solutions. The second table shows infusion rates in mL/min based on drug amount and patient weight (40 to 100 kg) for a 0.1 mg/mL solution. Notes clarify concentration and rate adjustments.*

FDA Label Image

Structure (Structure)

Chemical structure of vecuronium bromide showing its molecular configuration including nitrogen atoms and bromide ion as part of the compound.*

FDA Label Image

Vial Labeling (Vial Label)

Vecuronium Bromide for Injection 10 mg per vial lyophilized powder label for intravenous use. The label includes warnings about the drug being a paralyzing agent and for IV use only, with storage and reconstitution instructions. It is distributed by Auromedics Pharma LLC and made in the USA.*

* 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.