Sodium Bicarbonate Injection, Solution
Product Images NDC 51662-1573

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Bicarbonate (NDC 51662-1573). 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

Vial Label (51662 1573 1 Vial Label)

Vial Label (51662 1573 1 Vial Label)
Label for Sodium Bicarbonate Injection, USP, 8.4%, showing 50 mEq strength (1 mEq per mL) in a 50 mL single dose vial. The label states it is for intravenous use only and is marked Rx only. NDC 63323-089-50 is displayed at the top.*
FDA Label Image

How Supplied (How Supplied)

How Supplied (How Supplied)
A table listing Sodium Bicarbonate Injection, USP products including contents, NDC numbers, strengths, vial sizes, and pack sizes. It shows a 4.2% (42 mg/mL) strength in 5 mL flip-top single-dose vials, and an 8.4% (84 mg/mL) strength in 50 mL flip-top single-dose vials, both in packages of 25.*
FDA Label Image
FDA Label Image

Serialized Label (Serialized 51662 1573 1 1016520 Sodium Bicarb Hf Label Image (1))

Serialized Label (Serialized 51662 1573 1 1016520 Sodium Bicarb Hf Label Image (1))
A clear glass vial with a purple cap containing a solution labeled as 8.4% Sodium Bicarbonate Injection, USP. The label indicates the concentration as 50 mEq per 50 mL (1 mEq per mL) and states it is for intravenous use only. The vial is a 50 mL single-dose vial. It is distributed by HF Acquisition Co., 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.