Polymyxin B Injection, Powder, For Solution
Product Images NDC 0143-9941

3 FDA label images from Hikma Pharmaceuticals Usa 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 Polymyxin B (NDC 0143-9941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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.

FDA Label Image

Structural Formula (Polymyxin B For Injection Usp 1)

Structural Formula (Polymyxin B For Injection Usp 1)
Chemical structure diagram of Polymyxin B sulfate illustrating the molecular differences between Polymyxin B1 and Polymyxin B2 variants, highlighting amino acid sequences and structural groups.*
FDA Label Image

Vial (Polymyxin B For Injection Usp 2)

Vial (Polymyxin B For Injection Usp 2)
Polymyxin B for Injection, USP label for a 500,000 units per vial dosage form. This sterile injection powder from Hikma Pharmaceuticals USA Inc. is intended for hospital use only via intramuscular, intravenous, or intrathecal administration. The label includes dosage instructions, storage conditions, and a barcode.*
FDA Label Image

Shelfpack (Polymyxin B For Injection Usp 3)

Shelfpack (Polymyxin B For Injection Usp 3)
Polymyxin B injection, USP, 500,000 units per vial, powder for solution, labeled for intramuscular, intravenous, and intrathecal administration. The label indicates 10 sterile vials per package, for hospital use only. Manufactured by Hikma FarmacĂȘutica (Portugal) and distributed by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ.*

* 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.