Ephedrine Sulfate Injection
Product Images NDC 68083-495

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Ephedrine Sulfate (NDC 68083-495). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, 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

Ephedrine-spl-carton-label (Ephedrine Spl Carton Label)

Packaging label for Ephedrine Sulfate Injection, USP, 50 mg/mL, for intravenous use. The label states the product must be diluted and is supplied in 25 x 1 mL single-dose vials. It includes storage instructions, manufacturer details (Gland Pharma Limited, Hyderabad, India), and the NDC 68083-495. The design includes dosage and usage information along with a barcode and a diagram showing carton dimensions and packing details.*

FDA Label Image

Ephedrine-spl-container-label (Ephedrine Spl Container Label)

Label for Ephedrine Sulfate Injection, USP 50 mg/mL, a human prescription drug for intravenous use. The label indicates a 1 mL single-dose vial that must be diluted and discarded if unused. Manufactured by Gland Pharma Limited in Hyderabad, India, with an FDA NDC of 68083-495.*

FDA Label Image

Ephedrine-spl-structure (Ephedrine Spl Structure)

Chemical structure of Ephedrine Sulfate, showing the molecular arrangement of the ephedrine moiety and sulfate ion (H2SO4) in its dimeric form. The structure illustrates atoms and bonds characteristic of the compound.*

* 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.