Haloperidol Injection, Solution
Product Images NDC 55154-9553

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Haloperidol (NDC 55154-9553). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 107, 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.

FDA Label Image
FDA Label Image

Structure (Haloperidol Injection Usp Figure 1 Halo Struct)

Structure (Haloperidol Injection Usp Figure 1 Halo Struct)
Chemical structure of Haloperidol Lactate, showing the molecular formula C21H23ClFNO2 and molecular weight 375.86. The diagram depicts atoms and bonds corresponding to this active ingredient used in the injectable solution form.*
FDA Label Image

Bag Label (Image 01)

Bag Label (Image 01)
Label text panel for Haloperidol Injection USP 5 mg/mL solution, specifying a package of 5 single-dose 1 mL vials for intramuscular use. Includes dosage form, storage instructions (20° to 25°C, protect from light, do not freeze), warnings about non-child resistant packaging, and distribution details for Cardinal Health and Fresenius Kabi.*
FDA Label Image

Table

Table
A data table titled 'Adverse Reactions Occurring in ≥1% of Haloperidol-Treated Patients in Double-Blind, Parallel Placebo-Controlled Clinical Trials (Oral Haloperidol)' listing adverse reactions by system/organ class. It compares the percentage incidence of various gastrointestinal and nervous system disorders in patients treated with Haloperidol versus placebo, showing higher rates of extrapyramidal disorders in the Haloperidol group.*

* 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.