Bupivacaine Hydrochloride Injection, Solution
Product Images NDC 71872-7133

3 FDA label images from Medical Purchasing Solutions, Llc · 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 71872-7133). 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

Pdp (7133)

Pdp (7133)
Label of Bupivacaine Hydrochloride Injection 0.25% (2.5 mg/mL) multiple dose vial, 50 mL, for infiltration and nerve block use. Manufactured by Aurobindo Pharma Limited and repackaged by Medical Purchasing Solutions, LLC, Scottsdale AZ. The label includes dosage form, strength, lot and expiration placeholders, storage conditions, and preservative information.*
FDA Label Image

Package Label-principal Display Panel (0.25% 125 mg per 50 mL (2.5 mg/mL))

Package Label-principal Display Panel (0.25% 125 mg per 50 mL (2.5 mg/mL))
Bupivacaine Hydrochloride 2.5 mg/mL injection solution label. The product is a 50 mL multiple dose vial containing 125 mg per vial, indicated for infiltration and nerve block. It is sterile and nonpyrogenic, labeled for prescription use only. Manufactured for AuroMedics Pharma LLC by Aurobindo Pharma Limited.*
FDA Label Image

Bupivacaine Hydrochloride Chemical Structure (Bupivacaine Str)

Bupivacaine Hydrochloride Chemical Structure (Bupivacaine Str)
Chemical structure of Bupivacaine Hydrochloride, depicted with molecular groups including a piperidine ring, amide linkage, aromatic ring with methyl substitutions, 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.