Atropine Sulfate Injection
Product Images NDC 70518-4329

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 70518-4329). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm2 (Atropine Sulfate 8mg 20ml(0.4 mg mL) 70518 4329 01)

Atropine Sulfate Injection, 8 mg per 20 mL vial (0.4 mg/mL), multiple-dose vial. The label indicates this is for intravenous, intramuscular, subcutaneous, intraosseous, or endotracheal use. The manufacturer is RemedyRepack Inc., with reference to Hikma as the original manufacturer. The label includes storage instructions, a warning to discard within 24 hours of initial use, and a reminder to keep medication out of children's reach.*

FDA Label Image

Remedy_label (Remedy Label)

Atropine Sulfate 0.4 mg/mL injection supplied as 10 vials of 20 mL each, totaling 8 mg per vial. The label indicates it is for intravenous, intramuscular, subcutaneous, intraosseous, or endotracheal use. Packaged by RemedyRepack Inc., the label includes storage instructions and a discard warning after initial use.*

FDA Label Image

Atropine Sulfate Structural Formula (Atropine Sulfate Injection Usp Anda 1)

Chemical structure of Atropine Sulfate, showing the molecular arrangement including a tropane ring, ester linkage, aromatic ring, and associated sulfate and water molecules as indicated.*

* 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.