Ephedrine Sulfate Injection
Product Images NDC 55150-373

3 FDA label images from Eugia Us Llc · 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 Ephedrine Sulfate (NDC 55150-373). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eugia Us Llc, 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

Package Label-principal Display Panel-50 mg Per Vial (Container Label)

Package Label-principal Display Panel-50 mg Per Vial (Container Label)
Label for Ephedrine Sulfate Injection, USP, 50 mg/mL, intravenous use. The vial is single-dose and must be diluted before administration. Manufactured in India for AuroMedics Pharma LLC, East Windsor, NJ. The label includes barcode and directions to discard unused portion.*
FDA Label Image

Package Label-principal Display Panel-50 mg Per Vial (Container-Carton (25 Vial))

Package Label-principal Display Panel-50 mg Per Vial (Container-Carton (25 Vial))
Ephedrine Sulfate Injection, USP 50 mg per mL intravenous injection vial label. The label states it is for intravenous use and must be diluted. The package contains 25 single-dose 1 mL vials. Distributed by AuroMedics Pharma LLC, with storage instructions and additional details provided.*
FDA Label Image

Chemical-structure (Ephedrine Sulfate Str)

Chemical-structure (Ephedrine Sulfate Str)
Chemical structure of ephedrine sulfate showing the molecular arrangement with phenyl group, hydroxyl group, methyl group, and an ammonium group, associated with sulfuric acid (H2SO4). The structure depicts two ephedrine molecules complexed with one molecule of sulfuric acid.*

* 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.