Atropen Auto-injector Injection
Product Images NDC 11704-101

Product Visual Gallery

This gallery contains 24 technical images submitted to the FDA as part of the official labeling for Atropen Auto-injector (NDC 11704-101). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meridian Medical Technologies 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

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Chemical structure of atropine, showing its molecular framework including a tropane ring with an ester linkage to a bicyclic aromatic group and a hydroxyl functional group.*

FDA Label Image

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Packaging label for ATROPEN Auto-Injector containing 2 mg of atropine injection. The label is primarily green and yellow with directions indicating it is a single-dose auto-injector for intramuscular use in nerve agent and insecticide poisoning. The label includes safety release instructions and the manufacturer, Meridian Medical Technologies LLC.*

FDA Label Image

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Packaging label of ATROPEN Auto-Injector, a human prescription drug containing atropine injection for intramuscular use. The label indicates it as a single-dose auto-injector for intramuscular use only, intended for use in nerve agent and insecticide poisoning. The label shows safety removal instructions and is produced by Meridian Medical Technologies LLC.*

FDA Label Image

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The image shows the packaging label of ATROPEN Auto-Injector 0.5 mg atropine injection by Meridian Medical Technologies LLC. It is a single-dose auto-injector intended for intramuscular use, designed to remove a safety release after use. The label mentions its use in nerve agent and insecticide emergencies, highlighting that it contains 0.5 mg atropine sulfate in 0.7 mL solution.*

FDA Label Image

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Label of ATROPEN Auto-Injector showing multiple strengths of atropine injection (0.25 mg/0.3 mL, 0.5 mg/0.7 mL, 1 mg/0.7 mL, 2 mg/0.7 mL) for intramuscular use. The label highlights components such as the black tip and gray safety release, with Meridian Medical Technologies LLC as the labeler.*

FDA Label Image

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An instructional diagram showing hands administering an intramuscular injection using the ATROPEN Auto-Injector. The image illustrates the proper technique for holding and activating the auto-injector device labeled ATROPEN.*

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Illustration showing a hand holding an ATROPEN Auto-Injector highlighting two features: the yellow safety release at the top and the green tip at the bottom of the device.*

FDA Label Image

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An instructional illustration showing a hand pulling a yellow safety release from an ATROPEN Auto-Injector. The image highlights the action to remove the yellow safety device prior to use.*

FDA Label Image

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Illustration showing two methods of aid: Self Aid, depicting a person injecting themselves in the thigh; and Caregiver Aid, showing a person administering an injection to another seated individual, with arrows indicating injection sites and angles. This is an instructional diagram related to intramuscular injection administration.*

FDA Label Image

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An instructional illustration showing two methods of administering an intramuscular injection with the ATROPEN Auto-Injector. The left side depicts self-aid where the individual injects themselves into the outer thigh. The right side shows caregiver aid with another person assisting the injection into the patient's outer thigh while the patient is lying down.*

FDA Label Image

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An instructional illustration showing how to hold the ATROPEN Auto-Injector. The image depicts a hand gripping the injector with the thumb and fingers positioned for proper use, highlighting the device's angled cap.*

FDA Label Image

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An instructional illustration showing a hand holding an ATROPEN Auto-Injector with the green tip aimed downward, demonstrating the proper grip and positioning for intramuscular injection using this device.*

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An instructional illustration showing the usage steps of the ATROPEN Auto-Injector injection. It depicts a hand holding the auto-injector device, with another hand pulling off a safety cap, and then positioning the injector for intramuscular administration.*

FDA Label Image

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An instructional illustration showing a hand holding an ATROPEN Auto-Injector with labeled parts: a gray safety release at the top and a black tip at the bottom, indicating how to properly hold and operate the device for an intramuscular injection of atropine.*

FDA Label Image

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Instructional illustration showing how to remove the grey safety release from the ATROPEN Auto-Injector. The image depicts hands gripping the device and lifting the grey safety cap as a preparatory step before injection.*

FDA Label Image

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An instructional anatomical illustration showing the proper technique to administer an intramuscular injection using the ATROPEN Auto-Injector in the thigh area. The drawing highlights hand positioning and injection site on a human leg.*

FDA Label Image

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An instructional line drawing showing a person administering an intramuscular injection into the upper arm muscle of another individual. The illustration emphasizes hand positioning for injection technique, relevant for medicating with the ATROPEN Auto-Injector (atropine).*

FDA Label Image

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An instructional illustration showing a hand gripping an ATROPEN Auto-Injector syringe. The image depicts the proper way to hold the device, designed for intramuscular injection of atropine in various available strengths.*

FDA Label Image

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An instructional illustration showing a hand holding the ATROPEN Auto-Injector at the end of the arm, demonstrating the proper intramuscular injection technique. The injector is held firmly with the needle aimed outward from the hand.*

FDA Label Image

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Packaging label for ATROPEN (atropine injection) 0.25 mg single-dose auto-injector for intramuscular use by Meridian Medical Technologies LLC. The label includes storage instructions, manufacturer details, a barcode, and warnings not to touch the needle black tip. Illustrated four-step usage instructions for the auto-injector are also shown, including removing the safety release, positioning on the thigh, injection, and holding for 10 seconds while seeking medical attention.*

FDA Label Image

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Packaging label for ATROPEN Auto-Injector 0.5 mg atropine injection in a single-dose auto-injector for intramuscular use. The label states use for nerve agent and insecticide poisoning and includes illustrated instructions for use, warnings about handling the Green Tip and Yellow Safety Release, storage conditions, and manufacturer information for Meridian Medical Technologies LLC.*

FDA Label Image

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Packaging label for ATROPEN Auto-Injector 1 mg (atropine injection) intramuscular injection by Meridian Medical Technologies. The label highlights single-dose use for nerve agent and insecticide poisoning and provides usage instructions with illustrations, safety warnings, and storage conditions.*

FDA Label Image

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The packaging label for ATROPEN Auto-Injector 2 mg (atropine injection) depicts a single-dose auto-injector for intramuscular use by Meridian Medical Technologies LLC. The label highlights use for nerve agent and insecticide poisoning, dosage details, important safety instructions, and includes diagrams showing how to use the device, featuring components labeled as Yellow Safety Release and Green Tip.*

FDA Label Image

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Label for ATROPEN Auto-Injector containing atropine injection 2 mg, a single-dose auto-injector for intramuscular use in nerve agent and insecticide poisoning. The label includes storage instructions, usage directions with emphasis on placing the green end on the outer thigh, and manufacturer Meridian Medical Technologies LLC. Contains lot and expiration placeholders and multiple barcodes.*

* 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.