Dextrose Injection, Solution
Product Images NDC 51662-1215

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Dextrose (NDC 51662-1215). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

How Supplied (How Supplied)

Data table listing NDC numbers, container types, and sizes for Dextrose 25 g in 50 mL injection solution by HF Acquisition Co LLC. Container types include LifeShield Abboject Unit of Use Syringe with male luer lock and protected needle, Fliptop Vial, Ansyr Plastic Syringe, and Ansyr II Plastic Syringe with syringe and barrel detached.*

FDA Label Image

Logo (Logo)

FDA Label Image

Serialized Label (Serialized Label 51662 1215 1 Dextrose 50)

Dextrose 50% Injection, USP, 25 grams per 50 mL intravenous solution in a clear glass vial with a blue cap. The label includes dosage information and manufacturer details, Hospira, Inc., Lake Forest, IL, distributed by HF Acquisition Co., LLC, Mukilteo, WA. The vial is single-dose and marked for prescription use only.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of Dextrose illustrating its molecular arrangement, including hydroxyl groups and a water molecule (H2O), indicating it is likely the hydrated form.*

FDA Label Image

Vial Label (Vial Label)

Label for DEXTROSE 25 grams/50 mL (0.5 g/mL) Injection, USP, 50 mL single-dose vial. The label shows 50% dextrose concentration, intended for intravenous use. Manufactured by Hospira, Inc., Lake Forest, IL. Includes storage and usage information along with a barcode and National Drug Code (NDC) 0409-6648-02.*

* 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.