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.

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This text is likely a label or heading for a safety release mechanism, possibly colored yellow for high visibility. Additional context is needed to provide a more specific description.*

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This is a description for the product named Columbia B 31046, produced by Meridian Medical Technologies for Pfizer company. It is a single-dose auto-injector used primarily for intramuscular injection. It is used in the treatment of nerve agent and insecticide poisoning. The auto-injector delivers an injection of .021mg/0.3mL atropine, which is equivalent to 10025mg of atropine sulfate, 15mg of cic acid, and 20mg of sodium. It is important to not remove the product from its carton until required, and store it at a temperature between 15°C-30°C to prevent any damage. The product comes with a black tip, and it is important to not touch it with fingers to prevent any accident, as the needle extends rapidly from it. The product is manufactured only for intramuscular use and dosage as per the prescribing information.*

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The text is a set of instructions and information regarding the use of the ATROPEN Single-Dose Auto-Injector, which delivers an injection of atropine for intramuscular use. It includes warnings not to open the plastic sleeve or remove the injector until ready for use, not to remove the yellow safety release, and not to touch the green tip. The injector can be used through clothing, and medical attention must be sought immediately following injection. The text also provides details on the dosage and ingredients of the injection.*

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This text provides important instructions and information regarding the use of Atropen auto-injectors which contain atropine injection for nerve agent and insecticide poisoning. The text cautions against opening the plastic sleeve or removing the yellow safety release until ready for use, and warns against placing fingers on the green tip as the needle rapidly extends from it. Each injector delivers an injection of 0.84 mg/0.7 ml atropine sulfate, 12.5 mg glycerin, 2.7 mg citric acid monohydrate, 2.7 mg sodium citrate dihydrate, and 2.6 mg phenol. It is also mentioned that injecting through clothing is acceptable, however, immediate medical attention is advised following the injection.*

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This is a set of instructions for using the ATROPEN single-dose autoinjector, which contains 2mg of atropine for intramuscular use in case of nerve agent and insecticide poisoning. The autoinjector includes a yellow safety release, and the user should avoid touching the green tip as the needle extends rapidly. The injection can be given through clothing if necessary, and medical attention should be sought immediately afterward. The package includes information about the drug, and the autoinjector should be kept from freezing at temperatures below 15°C. The NDC number is 11704-106-01.*

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ATROPEN Single-Dose Auto-Injector is a medical technology produced by Pfizer for intramuscular use in nerve agent and insecticide poisoning. Each injector delivers 1.67mg/0.7mL of atropine sulfate. It should be stored at a temperature of 20°C-25°C, with permitted excursions to 15°C-30°C, and must be protected from freezing. The device is to be used by inserting the green end on the outer thigh and pushing hard until the injector functions. The product has NDC number 11704 10101 7 and should be handled with care.*

* 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.