Lidocaine Hydrochloride Injection, Solution
Product Images NDC 71872-7377

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lidocaine Hydrochloride (NDC 71872-7377). 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

7377.pdp (7377)

7377.pdp (7377)
Label for Lidocaine hydrochloride injection, USP 2% solution (20 mg/mL) in a 20 mL multiple-dose vial. The label indicates the product is for infiltration and nerve block use, not for caudal or epidural administration. Manufactured by Aspiro Pharma Limited and repackaged by Medical Purchasing Solutions, LLC. The label includes storage instructions and a list of inactive ingredients.*
FDA Label Image

7377m.pdp (7377m)

7377m.pdp (7377m)
Label for Lidocaine HCl Injection, USP 2% (20 mg/mL) in a 20 mL multiple dose vial by Camber Pharmaceuticals, Inc. The label states the product is sterile, nonpyrogenic, for infiltration and nerve block, excluding caudal or epidural use. It includes storage instructions, lot, and expiration placeholders, and manufacturer information for Camber Pharmaceuticals and Aspiro Pharma Limited.*
FDA Label Image
FDA Label Image
FDA Label Image

Lidocainestructure (Lidocainestructure)

Lidocainestructure (Lidocainestructure)
Chemical structure of Lidocaine hydrochloride, showing its molecular formula with aromatic ring, amide group, and hydrochloride component, corresponding to the active ingredient Lidocaine hydrochloride.*

* 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.