Bupivacaine Hydrochloride Injection, Solution
Product Images NDC 71872-7270

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Bupivacaine Hydrochloride (NDC 71872-7270). 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

71872-7270-1.pdp (71872 7270 1)

71872-7270-1.pdp (71872 7270 1)
Label for Bupivacaine Hydrochloride 0.5% Injection USP, 250 mg per 50 mL (5 mg/mL), in a 50 mL multiple dose vial. The label includes storage instructions, lot and expiration placeholders, and notes it is for nerve block only. Manufactured for AuroMedics Pharma LLC and repackaged by Medical Purchasing Solutions, LLC, Scottsdale, AZ.*
FDA Label Image

Package Label-principal Display Panel (0.5% 250 mg per 50 mL (5 mg/mL))

Package Label-principal Display Panel (0.5% 250 mg per 50 mL (5 mg/mL))
Bupivacaine Hydrochloride Injection USP 0.5% (5 mg/mL) in a 50 mL multiple dose vial. The label indicates the total drug content as 250 mg per 50 mL. It is marked for nerve block use and specifies it is not for caudal, epidural, or spinal anesthesia. Distributed by AuroMedics Pharma LLC.*
FDA Label Image

Bupivacaine Hydrochloride Chemical Structure (Bupivacaine Str)

Bupivacaine Hydrochloride Chemical Structure (Bupivacaine Str)
Chemical structure of bupivacaine hydrochloride showing its molecular components, including a piperidine ring, amide linkage, aromatic ring with methyl groups, and associated hydrochloride and water molecules.*

* 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.