Sodium Acetate Injection, Solution, Concentrate
Product Images NDC 80830-2435

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Sodium Acetate (NDC 80830-2435). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Private 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

1 (Sodium Acetate Injection 20 mL 1)

Label for Sodium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) intravenous solution concentrate. The label includes a caution statement to dilute before use, indicates a 20 mL single-dose vial, and provides storage instructions. It identifies Amneal Pharmaceuticals LLC as the distributor and includes product details such as sodium acetate concentration, pH range, and sterility. A barcode and placeholder for batch coding and expiration date are also visible.*

FDA Label Image

2 (Sodium Acetate Injection 20 mL 2)

Sodium Acetate Injection, USP 40 mEq/20 mL (2 mEq/mL) carton label for intravenous use. The label includes warnings stating "CAUTION: MUST BE DILUTED," the package contains 25 single-dose 20 mL vials, and is manufactured by Amneal Pharmaceuticals Pvt. Ltd., distributed by Amneal Pharmaceuticals LLC. It lists storage instructions, ingredient information, and the NDC 80830-2435.*

* 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.