Anthrasil Liquid
Product Images NDC 60492-0249

3 FDA label images from Emergent Biosolutions Canada Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Anthrasil (NDC 60492-0249). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Emergent Biosolutions Canada 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

Anthrasil Vial Label (Shelf Carton Label Ndc 60492 0249 2)

Anthrasil Vial Label (Shelf Carton Label Ndc 60492 0249 2)
Anthrasil 60 Units per vial intravenous liquid label for Anthrax Immune Globulin (human) by Emergent BioSolutions Canada Inc. The label notes storage at or below -15°C, no preservatives, and that the product is for intravenous use only with strategic national stockpile use. Distributed by CDC, includes barcodes and manufacturing details.*
FDA Label Image

Mean Tna Activities For Three Doses Of Anthrasil (Image 01)

Mean Tna Activities For Three Doses Of Anthrasil (Image 01)
A semi-logarithmic line graph showing mean TNA activity (mU/mL) over time (days post-dose) for three different Anthrasil doses: 210 U TNA, 420 U TNA, and 840 U TNA. The graph depicts decreasing TNA activity for each dose group across 0 to 84 days following administration.*
FDA Label Image

Anthrasil Carton Label (Image 02)

Anthrasil Carton Label (Image 02)
Anthrasil (Anthrax Immune Globulin Intravenous [human]) liquid intravenous plasma derivative, with a strength of 60 units per vial. The label shows storage instructions, manufacturer Emergent BioSolutions Canada Inc., distributor CDC, and specifies use only for the Strategic National Stockpile with 7 vials included.*

* 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.