Ethacrynate Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 69315-701

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ethacrynate Sodium (NDC 69315-701). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Leading Pharma, 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.

FDA Label Image

Chemicalstructure (Chemicalstructure)

Chemical structure diagram of ethacrynate sodium showing a chlorinated benzene ring with carboxyl and acrylate side groups, consistent with the active ingredient ethacrynate sodium used in injection form.*

FDA Label Image

Chemicalstructure1 (Chemicalstructure1)

Chemical structure of Ethacrynate Sodium showing a benzene ring with two chlorine substituents, an OCH2COONa group, and a COCH2CH3 substituent indicating its molecular composition.*

FDA Label Image

Containerlabel (Containerlabel)

Label for Ethacrynatate Sodium 50 mg/vial injection, USP, lyophilized powder for intravenous use. Single-dose vial packaging with dosing instructions, storage conditions, and preparation details. Manufactured for Leading Pharma, LLC with NDC 69315-701-50. Label includes barcode and 2D matrix code.*

FDA Label Image

Viallabel (Viallabel)

Label for ETHACRYNATE SODIUM Injection, USP 50 mg per vial, single-dose vial for intravenous use. The label states the active ingredient and strength, preparation instructions, storage conditions, and distributor information from Leading Pharma, LLC. It includes a UPC barcode and regulatory information.*

* 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.