Promethazine Hydrochloride Injection, Solution
Product Images NDC 39822-5550

3 FDA label images from Xgen Pharmaceuticals Djb, 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 Promethazine Hydrochloride (NDC 39822-5550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xgen Pharmaceuticals Djb, 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.

Product Images & Figures Index

FDA Label Image

Image (Promethazine HCl Injection 1)

Image (Promethazine HCl Injection 1)
Chemical structure of promethazine hydrochloride with molecular formula C17H20N2S·HCl and molecular weight 320.88. The diagram shows the arrangement of rings and atoms corresponding to the promethazine molecule plus the hydrochloride component.*
FDA Label Image

50mg/ml (Promethazine HCl Injection 2)

50mg/ml (Promethazine HCl Injection 2)
Label for PROMETHAZINE HYDROCHLORIDE Injection, USP 50 mg/mL in a 1 mL single dose ampul. The label notes protection from light and deep storage at room temperature. Manufactured for XGen Pharmaceuticals DJB, Inc. in Big Flats, NY, and made in Germany. Includes an NDC number 39822-5550-5 and barcode.*
FDA Label Image

Promethazine HCl Injection 3

Promethazine HCl Injection 3
Label for PROMETHAZINE HYDROCHLORIDE Injection, USP 50 mg/mL single dose ampuls, manufactured by XGen Pharmaceuticals DJB, Inc. The label indicates the product is for deep intramuscular use only and is supplied in a pack of 25 x 1 mL single dose ampuls. The product is manufactured in Germany and includes usage 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.