Atropine Sulfate
Product Images NDC 0409-4910

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 0409-4910). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Structural Formula Atropine Sulfate (Atropine 01)

Chemical structure diagram depicting the molecular formula of atropine sulfate monohydrate, the active ingredient in Atropine Sulfate products by Hospira, Inc. The diagram includes stereochemistry and functional groups characteristic of atropine sulfate.*

FDA Label Image

Hospira Logo (Atropine 02)

FDA Label Image

Principal Display Panel (10 mL Syringe Label)

Atropine Sulfate Injection USP 1 mg/10 mL (0.1 mg/mL) single-dose syringe label from Hospira, Inc. The label shows dosage strength, volume, NDC 0409-1630-15, and indicates intravenous use. It includes a barcode and space for lot and expiration dates.*

FDA Label Image

Principal Display Panel (10 mL Syringe Carton)

Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL) single-dose syringe label by Hospira, Inc. The 10 mL syringe label includes dosing strength, administration route for intravenous use, and instructions for aseptic technique. The label is primarily purple with black and red text detailing product information and handling instructions.*

FDA Label Image

Principal Display Panel (0.1 mg/mL Syringe Label)

Label for Atropine Sulfate Injection, USP Pediatric 0.25 mg/5 mL (0.05 mg/mL) in a 5 mL single-dose syringe. The label includes measurement markings in mL, NDC 0409-9630-15, and states 'For Intravenous Use.' The product is distributed by Hospira, Inc., Lake Forest, IL, and includes space for lot number and expiration date.*

FDA Label Image

Principal Display Panel (0.1 mg/mL Syringe Carton)

Packaging label for Pediatric Atropine Sulfate Injection, USP 0.25 mg/5 mL (0.05 mg/mL) by Hospira, Inc. The label indicates a 5 mL single-dose syringe for intravenous use, with directions for aseptic technique illustrated. The product is distributed by Hospira, Inc. and made in Spain.*

FDA Label Image

Principal Display Panel (0.05 mg/mL Syringe Label)

Atropine Sulfate 0.5 mg/5 mL (0.1 mg/mL) single-dose syringe label. The label indicates it is for intravenous use, Rx only, and includes the NDC 0409-4910-11. Distributed by Hospira, Inc., Lake Forest, IL. The label includes a dosage scale in milliliters and the Hospira logo.*

FDA Label Image

Principal Display Panel (0.05 mg/mL Syringe Carton)

Packaging label for Atropine Sulfate Injection, USP 0.5 mg/5 mL (0.1 mg/mL) by Hospira, Inc. The label indicates a 5 mL single-dose glass syringe with LIFESHIELD® ABBOJECT® technology, including a male luer lock adapter and 20-gauge protected needle. It includes handling instructions, storage information, usage warnings, expiration and lot number fields, and distributor information.*

FDA Label Image

Atropine 09

Atropine Sulfate 0.1 mg/mL injection label on a 10 mL single-dose syringe. The label shows the proprietary name Atropine Sulfate Injection, USP, with a strength of 1 mg per 10 mL (0.1 mg/mL), indicated for intravenous use. The product is distributed by Hospira, Inc. and includes an NDC number and barcode.*

FDA Label Image

Atropine 10

Packaging label for Atropine Sulfate Injection, USP 1 mg/10 mL (0.1 mg/mL) by Hospira, Inc. The label indicates a 10 mL glass single-dose syringe with LIFESHIELD ABBOJECT unit of use syringe, including a male luer lock adapter and 20-Gauge protected needle. Instructions for aseptic technique and syringe use are included, along with lot and expiration date placeholders. The label features cautions for handling and storage information.*

* 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.