Acetylcysteine
Product Images NDC 17478-660

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Acetylcysteine (NDC 17478-660). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, 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

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A line graph depicting plasma acetaminophen concentration (in µg/mL) over time (hours post-ingestion). The graph includes two labeled solid lines representing different thresholds (200 µg/mL at 4 hours and 150 µg/mL at 12 hours) used to assess hepatotoxicity risk. It indicates continuing acetylcysteine treatment if values fall on or above the solid line and likely hepatotoxicity if values fall above the solid line.*

FDA Label Image

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Chemical structure of acetylcysteine showing atomic connections and functional groups including amide, carboxyl, and thiol groups.*

FDA Label Image

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Acetylcysteine Injection label showing a strength of 6 g/30 mL (200 mg/mL) in a 30 mL single dose vial. The label indicates it must be further diluted prior to intravenous use. It is sterile, preservative free, and includes storage instructions at 20° to 25°C (68° to 77°F). Distributed by Akorn Operating Company LLC.*

FDA Label Image

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Acetylcysteine Injection 6 g/30 mL (200 mg/mL) preservative-free sterile solution label by Akorn. The label indicates it contains 4 single-dose 30 mL vials. It states the product must be further diluted prior to intravenous use and includes inactive ingredients and storage instructions. The NDC is 17478-660-30.*

* 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.