Ephedrine Sulfate Injection
Product Images NDC 72603-203

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 72603-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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 (Ca13c146 3b3f 41a8 8877 8451daaeea9b 01)

Structural Formula (Ca13c146 3b3f 41a8 8877 8451daaeea9b 01)
Chemical structure of ephedrine sulfate, showing two ephedrine molecules and one sulfuric acid (H2SO4) molecule.*
FDA Label Image

1 mL Vial Label (Ca13c146 3b3f 41a8 8877 8451daaeea9b 02)

1 mL Vial Label (Ca13c146 3b3f 41a8 8877 8451daaeea9b 02)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL in 1 mL single-dose vial. The label indicates the product is for intravenous use and must be diluted. Manufactured by Maiva Pharma Private Limited, India, and labeled for NorthStar Rx LLC, Memphis, TN. The label includes a barcode, lot number, and expiration date placeholders.*
FDA Label Image

25-count Carton Label (Ca13c146 3b3f 41a8 8877 8451daaeea9b 03)

25-count Carton Label (Ca13c146 3b3f 41a8 8877 8451daaeea9b 03)
Packaging label for Ephedrine Sulfate Injection, USP 50 mg/mL single-dose vials by NorthStar Rx LLC. The label includes warnings that the product must be diluted and is for intravenous use, discarding any unused portion. The package contains 25 vials of 1 mL each. Storage conditions and manufacturing details from Maiva Pharma Private Limited, India, are also shown.*

* 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.