Atropine Sulfate Solution
Product Images NDC 71872-7341

View Photos of 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 Atropine Sulfate (NDC 71872-7341). 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

7341.pdp (7341)

7341.pdp (7341)
Label for Atropine Sulfate Injection USP 0.4 mg/mL solution in a 1 mL single dose vial for intravenous use. The label includes product strength, dosage form, quantity (1 vial), storage instructions, manufacturer Somerset Therapeutics, LLC, and repackager Medical Purchasing Solutions, LLC Scottsdale, AZ.*
FDA Label Image

7341m.pdp (7341m)

7341m.pdp (7341m)
Atropine Sulfate Injection, USP 0.4 mg/mL solution for intravenous use in a 1 mL single-dose vial. The label states it is Rx only, with storage instructions to keep between 20° to 25°C and allows excursions between 15° and 30°C. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ; made in India. Includes barcode and packaging size 6.5 x 18 mm.*
FDA Label Image

Structure (7a8a5552 Fe21 4d36 8396 B7c99f41b4c4 01)

Structure (7a8a5552 Fe21 4d36 8396 B7c99f41b4c4 01)
Chemical structure of Atropine Sulfate, showing the detailed molecular arrangement including a bicyclic tropane ring with a methylamine group, ester linkage, and a phenyl ring, complexed with sulfuric acid and water molecules.*

* 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.