Atropine Sulfate Injection, Solution
Product Images NDC 0404-9802

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 0404-9802). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, 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

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Chemical structure diagram of Atropine Sulfate, showing its molecular components including a tropane ring and phenyl group, along with sulfate and water molecules.*

FDA Label Image

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A table titled "Table 1: Recommended Dosage" listing adult doses and repeat intervals for Atropine Sulfate injection. It includes uses such as antisialagogue or other antivagal (0.5 to 1 mg every 1 to 2 hours), organophosphorus or muscarinic mushroom poisoning (2 to 3 mg every 20 to 30 minutes), and bradyasystolic cardiac arrest (1 mg every 3 to 5 minutes, with a 3 mg maximum total dose).*

FDA Label Image

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A data table displaying concentration in mg/mL, package size, and corresponding NDC numbers for Atropine Sulfate injection. It lists 0.4 mg/mL and 1 mg/mL strengths, both available in packages of 25 vials, with their respective NDC codes 0517-1004-25 and 0517-1001-25.*

FDA Label Image

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FDA Label Image

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Atropine Sulfate 0.4 mg/mL injection, USP single-dose vial label for intravenous use. The label includes storage instructions (20 to 25°C), manufacturer Henry Schein, Inc., with address in Bastian, VA, and barcodes including NDC 0404-9802-01. It states to discard unused portion and keep out of children’s reach, marked RX ONLY.*

* 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.