Mepivacaine Injection, Solution
Product Images NDC 51004-0005

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Mepivacaine (NDC 51004-0005). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novocol Pharmaceutical Of Canada, Inc., 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

Principal Display Panel (1.7 mL Cartridge Carton)

Packaging label for Mepivacaine HCl 3% (30 mg/mL) Injection without Vasoconstrictor solution for submucosal injection. The label features the brand name Mepivacaine prominently, indicating a 50 single-dose cartridges pack of 1.7 mL each. It is labeled for dental block and infiltration use only, manufactured by Quala Dental Products, a Novocol Pharmaceutical of Canada, Inc. company. The design includes product and manufacturer information, barcodes, and the Quala Dental Products logo.*

FDA Label Image

Chemical Structure (Mepi 01)

Chemical structure of Mepivacaine Hydrochloride (C15H22N2·HCl) with molecular weight 282.81, showing the compound's ring and side groups as labeled.*

FDA Label Image

Chemical Structure (Mepi 02)

Chemical structure of Mepivacaine Hydrochloride, showing its molecular formula C9H13NO3 and molecular weight 183.21. The diagram includes functional groups and the molecular framework consistent with the active ingredient.*

FDA Label Image

Chemical Structure (Mepi 04)

Mepivacaine 30 mg/mL injection, solution in a clear glass vial with a metal cap and rubber stopper. The label on the vial shows the product name Mepivacaine Hydrochloride, strength as 30 mg/mL, and identifies the labeler as Novocol Pharmaceutical of Canada, Inc. The vial is intended for submucosal injection.*

* 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.