Pentamidine Isethionate Injection, Powder, Lyophilized, For Solution
Product Images NDC 13925-515

3 FDA label images from Seton Pharmaceuticals · 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 13925-515). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Seton Pharmaceuticals, 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

Carton Label

Carton Label
Packaging label for Pentamidine Isethionate for Injection, lyophilized powder, 300 mg per vial. The label specifies use for intramuscular or intravenous administration, with 10 single-dose vials per package. Manufactured by Seton Pharmaceuticals, the label includes dosage details, storage instructions, and a barcode, predominantly in green and red text on a white background.*
FDA Label Image

Pentam-structure (Cb8e8155 5505 44d5 9dee 525e2e45b95d 01)

Pentam-structure (Cb8e8155 5505 44d5 9dee 525e2e45b95d 01)
Chemical structure of Pentamidine Isethionate depicted as two aromatic rings connected by an ether linkage and including functional groups such as amidine and hydroxyl. The image also shows two isethionate groups associated with the compound and the molecular weight 592.68.*
FDA Label Image

Vial Label

Vial Label
Label for Pentamidine Isethionate injection, 300 mg per vial, lyophilized powder for solution. The label indicates it is preservative-free, sterile, nonpyrogenic, and intended for intramuscular or intravenous use. Manufactured by Seton Pharmaceuticals, LLC. Includes a barcode 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.