Structure (Ephedrine Sulfate Injection Usp 1)
Chemical structure diagram of ephedrine sulfate showing the molecular arrangement of the active ingredient.*
Ephedrine Sulfate Injection
Product Images NDC 0641-6238
4 FDA label images from Hikma Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 0641-6238). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
462-850-00 Sub 1 (Ephedrine Sulfate Injection Usp 2)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL, an intravenous injection provided by Hikma Pharmaceuticals USA Inc. The label indicates single-dose vial packaging of 1 mL, with instructions to dilute before intravenous use and discard any unused portion. It includes barcode and spaces for lot number and expiration date.*
462-851-00 Sub 1 (Ephedrine Sulfate Injection Usp 3)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL by Hikma Pharmaceuticals USA Inc. The image shows a vial label stating the product is for intravenous use, must be diluted, and unused portions should be discarded. It is supplied as 25 single-dose vials of 1 mL each. The label includes storage instructions and manufacturer details.*
Layout 1 Resized (Ephedrine Sulfate Injection Usp 4)
A small rectangular label featuring a QR code on the left side. The label includes text fields for GTIN, serial number (SN), expiration date (EXP), and lot number (LOT), with placeholder example values displayed. These identifiers are typically used for product tracking and verification.*
* 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.
