Bupivacaine Hydrochloride Injection
Product Images NDC 71351-022

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 71351-022). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Brookfield Pharmaceuticals, 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

Ampule-label-2ml (brookfield) (Ampoule Label 2ml (brookfield))

Label for Bupivacaine Hydrochloride 0.75% in Dextrose 8.25% Injection, USP, 2 mL ampule for spinal use. Contains 7.5 mg/mL bupivacaine HCl and 82.5 mg/mL dextrose. Distributed by Brookfield Pharmaceuticals, LLC. Displays NDC 71351-022-02, barcode, and placeholders for lot number and expiration date.*

FDA Label Image

Bupivacaine Formula (Bupivacaine Formula)

Chemical structure of Bupivacaine hydrochloride showing the molecular arrangement, including the piperidine ring, amide linkage, aromatic ring with methyl groups, and associated hydrochloride and hydration components.*

FDA Label Image

Carton-label-50amp (brookfield) (Carton Label 50amp (brookfield))

Packaging label for Bupivacaine Hydrochloride in Dextrose Injection, USP 0.75% (7.5 mg/mL) and 8.25%. The label indicates it is a sterile hyperbaric solution for spinal anesthesia, supplied as 50 single-dose 2 mL ampules. Distributed by Brookfield Pharmaceuticals, LLC, made in South Korea. The label includes storage instructions and lot/expiration date areas.*

FDA Label Image

Dextrose Formula (Dextrose Formula 1)

Chemical structure diagram of bupivacaine hydrochloride showing molecular components and a water molecule (H2O).*

* 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.