Atropine Sulfate Injection, Solution
Product Images NDC 51662-1627

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atropine Sulfate (NDC 51662-1627). 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

Dosage (Dosage)

Dosage (Dosage)
A table titled 'Recommended Dosage' showing adult use cases and doses for Atropine sulfate injection. It lists uses such as anticholinergic or antiviral, organophosphorus or muscarinic mushroom poisoning, and bradyasystolic cardiac arrest, with corresponding doses and repeat intervals.*
FDA Label Image

Serialized (Serialization Label)

Serialized (Serialization Label)
Package label for Atropine sulfate injection solution distributed by HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA. The label includes barcode data and instructs to see the manufacturer's package insert. It is marked RX only.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of atropine sulfate, showing the bicyclic tropane ring linked to an ester and a phenyl group, with sulfate and water molecules indicated.*
FDA Label Image

Vial (Vial Label)

Vial (Vial Label)
Atropine Sulfate Injection, USP 0.4 mg/mL, sterile solution for intravenous use in a 1 mL single-dose vial. The label includes directions for recommended storage temperatures and indicates to discard any unused portion. The labeler is HF Acquisition Co LLC, DBA HealthFirst.*

* 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.