Sodium Ferric Gluconate Complex In Sucrose Injection
Product Images NDC 0143-9298

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Sodium Ferric Gluconate Complex In Sucrose (NDC 0143-9298). 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.

FDA Label Image

Novaplus Container Label (Sodium Ferric Gluconate Complex In Sucrose Injecti 1)

Label for Sodium Ferric Gluconate Complex in Sucrose Injection containing 62.5 mg elemental iron per 5 mL (12.5 mg/mL) in a 5 mL single-dose vial. The injection is for intravenous use only and distributed by Hikma Pharmaceuticals USA Inc. Storage instructions specify 20° to 25°C (68° to 77°F).*

FDA Label Image

Novaplus Shelfpack (Sodium Ferric Gluconate Complex In Sucrose Injecti 2)

Label for Sodium Ferric Gluconate Complex in Sucrose Injection 12.5 mg/mL by Hikma Pharmaceuticals USA Inc. It indicates 62.5 mg elemental iron per 5 mL (12.5 mg/mL) in a package of 10 single dose vials. The label notes the product is for intravenous use only and includes storage instructions at 20° to 25°C. Additional inactive ingredient and dosage information are partially visible.*

FDA Label Image

Sodium Ferric Gluconate Complex In Sucrose Injecti 3

Packaging label for Sodium Ferric Gluconate Complex in Sucrose injection, showing a QR code and text fields for GTIN, serial number, expiration date, and lot number. The label is from Hikma Pharmaceuticals USA Inc. and includes placeholders for product identification details but does not show strength or dosage form details.*

* 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.