Ephedrine Sulfate Injection
Product Images NDC 71872-7276

3 FDA label images from Medical Purchasing Solutions, 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 71872-7276). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

Chemical-structure (Ephedrine Sulfate Str)

Chemical-structure (Ephedrine Sulfate Str)
Chemical structure of ephedrine sulfate, depicting the molecular arrangement of ephedrine combined with sulfuric acid (H2SO4). The structure shows two ephedrine molecules paired with one sulfuric acid molecule in the compound.*
FDA Label Image

Ephevial (Ephevial)

Ephevial (Ephevial)
Ephedrine Sulfate Injection, USP 50 mg per mL label for intravenous use. The single-dose vial contains 1 mL and must be diluted before administration. Manufactured in India for AuroMedics Pharma LLC, East Windsor, NJ. Includes barcode and storage instructions to discard unused portion.*
FDA Label Image

Ephelabel (Ephelabel)

Ephelabel (Ephelabel)
Label for Ephedrine Sulfate Injection USP, 50 mg/mL, 1 mL single-dose vial. For intravenous use, must be diluted. The label includes storage instructions (20 to 25 °C, excursions permitted from 15 to 30 °C), manufacturer and distributor information: Manufactured by AuroMedics Pharma LLC, made in India, repackaged and distributed by Medical Purchasing Solutions, LLC in Scottsdale, AZ. The vial does not contain natural rubber latex.*

* 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.