Atropine Sulfate Solution
Product Images NDC 71872-7355

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 71872-7355). 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

Image (125328fe C82b 42fd Bb3b Ba3f6c125ced 14)

Chemical structure of Atropine Sulfate monohydrate, showing the molecular arrangement including the tropane ring, phenyl group, sulfate, and water molecules associated as hydrate.*

FDA Label Image

7355.pdp (7355)

Atropine Sulfate Injection USP, 8 mg/20 mL (0.4 mg/mL) solution vial. The label specifies intravenous, intramuscular, subcutaneous, intraosseous, or endotracheal use. It lists active and inactive ingredients including atropine sulfate, benzyl alcohol, and sodium chloride. Storage instructions note 20° to 25°C controlled room temperature. Manufactured for Medical Purchasing Solutions, LLC, Scottsdale, AZ, repackaged in India.*

FDA Label Image

7355m.pdp (7355m)

Label for Atropine Sulfate Injection, USP, 0.4 mg/mL solution in a 20 mL multiple-dose vial. The label indicates it is for intravenous, intramuscular, subcutaneous, intraosseous, or endotracheal use. The product is prescription-only and manufactured for Somerset Therapeutics, LLC by a facility in India. The label includes ingredient and dosage details as well as 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.