Ephedrine Sulfate Injection
Product Images NDC 71872-7269

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This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 71872-7269). 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.

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FDA Label Image

71872-7269-1.pdp (71872 7269 1)

71872-7269-1.pdp (71872 7269 1)
This is a description of Ephedrine Sulfate Injection, USP, which is a medication that requires dilution before intravenous use. It comes in a single-dose vial containing 80 mg/mL of ephedrine sulfate and should be discarded if any portion is not utilized. Each mL contains 50 mg of ephedrine sulfate and water for injection. The injectable solution has a pH range of 4.5 to 7.0, adjusted with either sodium hydroxide and/or acetic acid. The package insert contains usage instructions, and it must be stored between 20° and 25°C (68° to 77°F) but can be excursed between 15° to 30°C (59°to 86°F) [as per USP Controlled Room Temperature]. The vial stoppers do not contain natural rubber latex. It is manufactured in India by Amneal Pharmaceuticals Pvt. Ltd. Parental Unit Ahmedabad 3882213, and distributed in the USA by Amneal Pharmaceuticals LLC Bridgewater, NJ 08807. It is repackaged and distributed by a company named Medicel Purchasing Solutions in Scottsdale, AZ85260.*
FDA Label Image

L (Ephedrine Sulfate Injection 1)

L (Ephedrine Sulfate Injection 1)
FDA Label Image

1 (Ephedrine Sulfate Injection 2)

1 (Ephedrine Sulfate Injection 2)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.