Acetaminophen Injection, Solution
Product Images NDC 55579-405

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acetaminophen (NDC 55579-405). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Solupharm Pharmazeutische Erzeugnisse Gmbh, 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

Label (Label)

Label for Acetaminophen Injection 10 mg/mL (1000 mg/100 mL) solution for intravenous use. The label states it is a single use vial, 100 mL in volume, for prescription use only. It includes storage instructions (20° to 25°C), ingredients, manufacturer information (Solupharm GmbH, Germany), and distributor (Leucadia Pharmaceuticals, Carlsbad, CA). A barcode and lot/expiration date fields are also visible.*

FDA Label Image

Label2 (Label2)

Label for Acetaminophen Injection 1000 mg/100 mL (10 mg/mL) intravenous solution. The label states single-use vials with 24 x 100 mL vials. It includes storage instructions, active ingredient details, manufacturer information listing Solupharm GmbH and Leucadia Pharmaceuticals, and barcode. The product is Rx only and made in Germany.*

FDA Label Image

Chemical Structure (Image 1 Structure)

Chemical structure of acetaminophen showing the aromatic ring with a hydroxyl group and the acetamide functional group attached.*

FDA Label Image

Figure 1 (Image 2 Fig 1)

A line graph depicting mean temperature (°C) versus time post dose (hours) comparing intravenous acetaminophen and placebo. The graph shows temperature changes over a 6-hour period, with separate lines representing IV acetaminophen and placebo groups.*

* 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.