Cosyntropin Injection, Powder, Lyophilized, For Solution
Product Images NDC 71872-7313

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cosyntropin (NDC 71872-7313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

7313.pdp (7313)

Label for Cosyntropin injection, powder, lyophilized for solution, 0.25 mg per 1 mL single-dose vial. The label indicates RX only status and states the vial is for intravenous or intramuscular use. It details that the vial contains Cosyntropin 0.25 mg (approx. 0.25 USP Unit ACTH) with Mannitol 10 mg, to be reconstituted with 1 mL of 0.9% sodium chloride injection. The label includes storage instructions at 20°C (68° to 77°F) and manufacturer information, repackaged by Medical Purchasing Solutions, Scottsdale, AZ.*

FDA Label Image

7313.jpg (73131)

Cosyntropin injection label for 0.25 mg per vial in lyophilized powder form for intravenous use. The label indicates it is for diagnostic use only and requires reconstitution before administration. Manufactured by Medical Purchasing Solutions, LLC, with storage instructions and lot/expiration date fields present. Branding includes 'Sandoz'.*

FDA Label Image

Image 1 (Image 01)

A linear sequence of amino acids representing the peptide structure of Cosyntropin, listing each amino acid with its three-letter abbreviation and position from 1 to 24.*

* 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.