Atropine Sulfate Injection
Product Images NDC 71872-7252

3 FDA label images from Medical Purchasing Solutions, Llc · Packaging, Regulatory Labels, and Product Appearance

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)
Label for Atropine Sulfate Injection USP 1 mg/10 mL (.1 mg/mL) in a Luer-Jet Luer-Lock prefilled syringe. The label indicates this product is for intravenous use, single-dose syringe with instructions to discard unused portion. It is repackaged and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ, and manufactured by International Medication Systems, El Monte, CA.*
FDA Label Image

Mm1 (Carton1)

Mm1 (Carton1)
Atropine Sulfate Injection, USP 1 mg per 10 mL (0.1 mg/mL) in a single-dose Luer-Jet Luer-Lock prefilled syringe label. The packaging indicates it is for intravenous use only, supplied by Medical Purchasing Solutions, LLC, NDC 76329-3340-1. The label includes dosage instructions and cautions for use and disposal.*
FDA Label Image

Structure1 (Structure1)

Structure1 (Structure1)
Chemical structure diagram of Atropine Sulfate, showing its molecular framework with labeled carbon, hydrogen, nitrogen atoms, and associated sulfate and water components.*

* 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.