Pentamidine Isethionate
Product Images NDC 39822-3050

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 Pentamidine Isethionate (NDC 39822-3050). 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

Penj-cm-01 (Penj Cm 01)

Penj-cm-01 (Penj Cm 01)
Label for Pentamidine Isethionate for Injection 300 mg per vial by XGen Pharmaceuticals DJB, Inc. The label indicates it is a lyophilized product for intramuscular or intravenous use, with 10 single-dose vials. It includes administration instructions, storage conditions, preservative information, and a barcode. The product is manufactured in Big Flats, NY.*
FDA Label Image

Penj-vl-01 (Penj Vl 01)

Penj-vl-01 (Penj Vl 01)
Label for PENTAMIDINE ISETHIONATE sterile preservative-free lyophilized powder for injection, 300 mg per vial. Manufactured by XGen Pharmaceuticals DJB, Inc. The label includes instructions for reconstitution with sterile water or 5% dextrose injection for intramuscular or intravenous use. The label also notes storage conditions, usage as a single-dose vial, and disposal instructions for unused portions.*
FDA Label Image

Structural Formula (Structural Formula 2)

Structural Formula (Structural Formula 2)
Chemical structure of pentamidine isethionate showing its molecular composition with formula C19H24N4O2ยท2C2H6O4S and molecular weight of 592.68.*

* 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.