Ephedrine Sulfate Injection
Product Images NDC 36000-336

View Photos of 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 36000-336). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Logo_image (Image 02)

FDA Label Image

Image01-structural-formula (Image01 Structural Formula)

Image01-structural-formula (Image01 Structural Formula)
Chemical structure of ephedrine sulfate showing its molecular arrangement including a phenyl ring, hydroxyl group, methyl group, amine group, and sulfate component.*
FDA Label Image

Image02-container (Image02 Container)

Image02-container (Image02 Container)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL, a prescription intravenous injection manufactured for Baxter Healthcare Corporation. The label indicates it is a 1 mL single-dose vial that must be diluted before use. The product is made in India and includes lot and expiration placeholders, along with a barcode and manufacturing details.*
FDA Label Image

Image03-carton (Image03 Carton)

Image03-carton (Image03 Carton)
Label for Ephedrine Sulfate Injection, USP 50 mg/mL by Baxter Healthcare Corporation. It is an intravenous injection supplied as 25 x 1 mL single-dose vials. The label states the product must be diluted before use and discards any unused portion. Manufactured by Baxter Pharmaceuticals India Pvt Ltd for Baxter Healthcare Corporation, Deerfield, IL.*

* 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.