Ephedrine Sulfate Injection
Product Images NDC 70700-249

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 70700-249). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xiromed, 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

Principal Display Panel (10 x 1 Ampule Carton)

Ephedrine Sulfate Injection, USP 50 mg/mL carton label for 10 x 1 mL single-dose vials, intended for intravenous use and must be diluted. The label includes NDC 70700-249-23, the Xiromed LLC labeler name, and storage instructions. The package is marked Rx Only.*

FDA Label Image

Principal Display Panel (25 x 1 mL Ampule Carton)

Box label for Ephedrine Sulfate Injection, USP 50 mg/mL by Xiromed, LLC. The label states the product is for intravenous use and must be diluted. The package contains 25 single-dose 1 mL vials. Storage instructions and ingredient information are included, along with barcode and manufacturer details indicating it is made in India.*

FDA Label Image

Chemical Structure (Ephedrine Sulfate Injection Chemical Stucture)

Chemical structure depicting ephedrine sulfate, showing the ephedrine molecule complexed with sulfuric acid (H2SO4).*

FDA Label Image

Principal Display Panel (1 mL Ampule Cantainer)

Label for Ephedrine Sulfate Injection, USP 50 mg/mL, an intravenous injection in a 1 mL single-dose vial. The label includes usage directions such as dilution requirement and storage conditions, and identifies the manufacturer as Xiromed, LLC, Florham Park, NJ. The product is designated Rx Only with NDC 70700-249-22.*

* 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.