Sodium Bicarbonate Injection, Solution
Product Images NDC 63323-089

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Sodium Bicarbonate (NDC 63323-089). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Package Label (PRINCIPAL DISPLAY – Sodium Bicarbonate 4.2% Single Dose Vial Label)

Sodium Bicarbonate Injection, USP, 4.2% with a strength of 2.5 mEq (0.5 mEq per mL) in a 5 mL single dose vial. The label states it is for intravenous use only and is designated Rx only. The NDC on the label is 63323-083-05.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sodium Bicarbonate 8.4% Single Dose Vial Label)

Label for Sodium Bicarbonate Injection USP, 8.4%, containing 50 mEq (1 mEq per mL) in a 50 mL single dose vial. The product is for intravenous use only and is prescription only. The NDC code 63323-089-50 and the labeler Fresenius Kabi USA, LLC are indicated.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sodium Bicarbonate 4.2% Single Dose Tray Label)

Label for Sodium Bicarbonate Injection, USP, 4.2% (0.5 mEq per mL) in a package of 25 single-dose vials, each containing 5 mL. The product is for intravenous use only and is prescription-only, labeled by Fresenius Kabi USA, LLC.*

FDA Label Image

Logo (Sod0d 0005 04)

Sodium Bicarbonate 42 mg/mL intravenous injection solution carton label. The packaging is from Fresenius Kabi USA, LLC, Lake Zurich, IL. The label includes product and labeler information with the Fresenius Kabi logo in black on a white background.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Sodium Bicarbonate 8.4% Single Dose Tray Label)

Sodium Bicarbonate Injection, USP, 8.4%, 50 mEq (1 mEq per mL) for intravenous use. The label indicates package contains 25 single dose vials of 50 mL each. Product is for prescription use only and labeled with NDC 63323-089-50 by Fresenius Kabi USA, LLC.*

* 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.