Atropine Sulfate Injection
Product Images NDC 71872-7252

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 71872-7252). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7252-1.pdp (71872 7252 1)

71872-7252-1.pdp (71872 7252 1)
This is a description of Atropine Sulfate Injection, USP in a pre-filled syringe for intravenous use. Each mL contains 0.1 mg atropine sulfate monohydrate, equivalent to 0.083 mg atropine with may contain sodium hydroxide and/or sulfuric acid for pH adjustment. The air above the liquid in the container is displaced by nitrogen gas, and the medication and fluid pathway is sterile and non-pyrogenic. The usual dosage must be based on the prescribing information. The unused portion of the single-dose syringe must be discarded. The medicine should be stored between 20°C to 25°C (68°F to 77°F) with permitted excursions between 15°C and 30°C (59°F to 86°F). The product is manufactured by International Medication Systems, and this particular syringe is repackaged and distributed by an entity called "Medical Purchasing Solutions" in Scottsdale, AZ.*
FDA Label Image

Mm1 (Carton1)

Mm1 (Carton1)
Atropine Sulfate Injection, USP is a medication used for various medical conditions. It comes in a concentration of 1mg/10mL (0.1 mg/mL) and may contain certain substances like atropine sulfate and menohydste. It is usually placed in a package with different components and should be used carefully.*
FDA Label Image

Structure1 (Structure1)

* 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.