Ephedrine Sulfate Injection
Product Images NDC 65219-257

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 65219-257). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Structural Formula (Eph09 0000 01)

Chemical structure diagram of Ephedrine Sulfate, showing two ephedrine molecules and one sulfate ion, corresponding to the molecular components of the drug's active ingredient.*

FDA Label Image

Logo (Eph09 0000 02)

Ephedrine Sulfate 50 mg/mL injection vial label from Fresenius Kabi USA, LLC. The vial contains clear liquid and is designed for intravenous use. Text on the label includes the product name, strength, and dosage form.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ephedrine Sulfate 50 mg/mL Shelf Carton)

Packaging label for Ephedrine Sulfate Injection, USP 50 mg/mL, an intravenous injection. The label indicates the product is supplied as 25 single-dose 1 mL vials and must be diluted before use. The labeler is Fresenius Kabi USA, LLC, with manufacturing information from UBI Pharmaceuticals, Inc. The label includes a blue and white color scheme with dose and usage details prominently displayed.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Ephedrine Sulfate 50 mg/mL Vial Label)

Label for Ephedrine Sulfate Injection, USP 50 mg/mL from Fresenius Kabi USA, LLC. It is an intravenous injection presented in a 1 mL single-dose vial. The label notes the product must be diluted and unused portions discarded. The label includes an NDC barcode and manufacturing origin listed as Taiwan.*

* 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.