Ephedrine Sulfate Injection
Product Images NDC 71872-7257

View Photos of 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 71872-7257). 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

71872-7257-01.pdp (71872 7257 01)

71872-7257-01.pdp (71872 7257 01)
Label for Ephedrine Sulfate Injection USP 50 mg/mL, a 1 mL single-dose vial for intravenous use. The label includes dilution instructions, storage conditions, and manufacturer information. It is repackaged and distributed by Medical Purchasing Solutions, LLC, Scottsdale, AZ. The label displays the NDC 71872-7257-1 and states vial stoppers do not contain natural rubber latex.*
FDA Label Image

L (Ephedrine Sulfate Injection 1)

L (Ephedrine Sulfate Injection 1)
Chemical structure of ephedrine sulfate showing the molecular arrangement of ephedrine ions and sulfate ions (SO4 2-). The diagram depicts stereochemistry with chiral centers and associated functional groups.*
FDA Label Image

1 (Ephedrine Sulfate Injection 2)

1 (Ephedrine Sulfate Injection 2)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL intravenous injection in a 1 mL single-dose vial. The label states it must be diluted for intravenous use and unused portion discarded. Distributed by Amnea Pharmaceuticals LLC, Bridgewater, NJ. Includes barcode and manufacturing information.*

* 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.