Atropine Sulfate Injection, Solution
Product Images NDC 0404-9784

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 0404-9784). 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 of atropine sulfate, showing the atropine molecule complexed with sulfuric acid (H2SO4) and water (H2O) components in a 2:1 ratio.*

FDA Label Image

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A data table outlining adult dosing guidelines for atropine sulfate injection. It lists uses such as antisialagogue or antivagal effects, organophosphorus or muscarinic mushroom poisoning, and bradyasystolic cardiac arrest. For each use, the table provides dose ranges and recommended repeat intervals.*

FDA Label Image

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A data table listing Atropine Sulfate Injection USP strengths and related NDC codes. It shows 0.5 mg/5 mL (0.1 mg/mL) strength, NDC 70121-1705-7 for a package of ten 5 mL single-dose glass syringes, and NDC 70121-1705-1 for a single syringe in one carton.*

FDA Label Image

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Data table presenting NDC numbers and packaging details for Atropine Sulfate Injection USP at 1 mg/10 mL (0.1 mg/mL). It lists unit of sale options as packages of 10 or 24 single-dose 10 mL glass syringes, and individual syringes in single cartons.*

FDA Label Image

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Label for Atropine Sulfate Injection, USP, 0.5 mg/5 mL (0.1 mg/mL) single-dose syringe by Henry Schein, Inc. The label includes usage instructions for intravenous use, cautions about glass liquid, storage temperature, and barcodes. It specifies handling instructions, lot and expiration placeholders, and the company address in Bastian, VA.*

* 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.