Atropine Sulfate Injection, Solution
Product Images NDC 51662-1626

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 51662-1626). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Serialized Label (51662 1626 1)

Data matrix barcode label including human prescription drug information for Atropine Sulfate injection solution. The label shows GS1 and serial number codes, a lot number, and instructions to see the manufacturer's package insert. Distributed by HF Acquisition Co., LLC in Mukilteo, WA. No proprietary branding or strength visible on this label portion.*

FDA Label Image

Dosage (Dosage)

A table titled 'Recommended Dosage' presenting dosage guidelines for adults for ATROPINE SULFATE. It lists uses including antisialagogue or other antivagal, organophosphorus or muscarinic mushroom poisoning, and bradyasystolic cardiac arrest, with corresponding doses and repeat intervals.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of atropine sulfate, showing the molecular arrangement including the bicyclic tropane ring bound to a tropic acid ester, with sulfate and water molecules indicated in the structure.*

FDA Label Image

Vial (Vial Label)

Label for Atropine Sulfate Injection, USP 1 mg/mL single-dose vial. The label indicates the product is sterile for intravenous use, with instructions to discard unused portions. It includes storage temperature guidelines and is labeled by American Regent, Inc., Shirley, NY.*

* 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.