Sodium Bicarbonate Injection, Solution
Product Images NDC 71872-7266

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Bicarbonate (NDC 71872-7266). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7266-1.pdp (71872 7266 1)

This is a description of a medical product called NI Beom which is a 8.4% Sodium Bicarbonate Injection, USP used for intravenous purposes. Each mL contains 84mg of sodium bicarbonate and is stored in a glass ABBOJECT® Unit of Use Syringe with male luer lock adapter and 18-Gauge protected needle for single-dose use. The product needs to be stored away from freezing temperatures and should not be used if it contains precipitate. Manufacturer of this product is Hospira, Inc., Lake Forest and it is distributed by Repackaged Medical Purchasing Solutions from Scottsdale, AZ.*

FDA Label Image

Hospira Logo (Sodium 01)

FDA Label Image

Hospira Logo (Sodium 02)

FDA Label Image

Principal Display Panel (1 mEq/mL Syringe Label)

This is a description of a solution of 8.4% sodium bicarbonate injection, with a strength of 50 mEq/50mL (1 mEq/mL). The solution is intended for intravenous use and is sterile and non-pyrogenic. The usual dosage information is included in the insert. The solution comes in a 50 mL single-dose bottle with a National Drug Code (NDC) of 0409-6637-24. The pH of the solution is 8.0 (7.0 to 8.5) and its osmolality is 1.56 mOsmol/mL. This product is manufactured by Hospira Inc., located in Lake Forest, IL.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.