Vecuronium Bromide
Product Images NDC 51662-1475

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Vecuronium Bromide (NDC 51662-1475). 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

Boxed Warning (Boxed Warning)

A warning panel stating that the drug VECURONIUM BROMIDE should be administered only by individuals adequately trained and familiar with its actions, characteristics, and hazards. The text appears prominently within a rectangular border.*

FDA Label Image

Dosage 1 (Dosage 1)

A data table presenting infusion delivery rates for Vecuronium Bromide. It shows drug delivery rates in mcg/kg/min and corresponding infusion delivery rates in mL/kg/min for two concentrations: 0.1 mg/mL and 0.2 mg/mL. Additional notes indicate 10 mg and 20 mg of vecuronium bromide in 100 mL solution, respectively.*

FDA Label Image

Dosage 2 (Dosage 2)

A data table showing the infusion rate of Vecuronium Bromide in mL per minute based on patient weight in kilograms. The table correlates drug amount in mcg/kg/min with patient weights ranging from 40 to 100 kg, providing specific infusion rates for each weight and dosage combination.*

FDA Label Image

Hs Logo (How Supplied Logo)

FDA Label Image

How Supplied (How Supplied)

A data table listing two NDC numbers (0409-1632-01 and 0409-1634-01) with descriptions for vecuronium bromide: 10 mg in 10 mL Fliptopt vials and 20 mg in 25 mL Fliptopt vials. Both descriptions note that diluent is not supplied.*

FDA Label Image

Logo (Logo)

FDA Label Image

Serialized Vial Labeling (Serialized Vial)

VECURONIUM BROMIDE injection vial with a red cap. The label indicates the product is for injection and includes a 10 mg strength noted in red. The vial also displays distribution information and a barcode. The labeler is HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Structure (Structure)

Chemical structure of Vecuronium Bromide showing its steroidal framework with multiple rings, acetyl groups, and two nitrogen-containing piperidine rings along with a bromide ion.*

FDA Label Image

Vial Label Opt. 1 (Vial Label Opt 1)

Label for Vecuronium Bromide for Injection, 10 mg per vial, for intravenous use only. The label includes warnings about its paralyzing effects and respiratory arrest risk, usage instructions to protect from light, and preparation details for reconstitution. It is distributed by Hospira, Inc., Lake Forest, IL, USA. The label also shows an NDC 0409-1632-21 and batch information.*

FDA Label Image

Vial Label Opt. 2 (Vial Label Opt 2)

Label for Vecuronium Bromide for Injection, with a strength of 10 mg* per 10 mL (1 mg/mL when reconstituted). It is indicated for intravenous use only and protected from light. The label features warnings about its paralytic effects, instructions for reconstitution, and storage guidelines. The product is distributed by Hospira, Inc., and includes space for batch information and dates.*

FDA Label Image

Vial Label Opt. 3 (Vial Label Opt 3)

Vecuronium Bromide for Injection label showing 10 mg strength for IV use only. The vial or packaging includes warnings about respiratory depression and instructions for reconstitution with bacteriostatic water or sterile water for injection. The label also advises protecting the product from light and notes storage instructions with discard guidelines. Manufacturer listed as Hospira, Inc.*

* 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.