Nalbuphine Hydrochloride Injection, Solution
Product Images NDC 71872-7114

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Nalbuphine Hydrochloride (NDC 71872-7114). 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 (7114)

Nalbuphine Hydrochloride Injection, 10 mg/mL, 10 mL multiple-dose vial label. The drug is indicated for intravenous, intramuscular, or subcutaneous use. The label includes storage instructions, a list of inactive ingredients, manufacturer information (Hospira, Inc.), and repackager details (Medical Purchasing Solutions, LLC, Scottsdale, AZ). It features a barcode, lot number, and expiration date placeholders.*

FDA Label Image

Chemical Structure (Nalbuphine 01)

Chemical structure diagram of Nalbuphine Hydrochloride, showing the molecular framework with labeled components including hydroxyl groups, nitrogen, and cycloalkane rings, with an HCl molecule indicated separately.*

FDA Label Image

Logo (Nalbuphine 02)

FDA Label Image

Principal Display Panel (10 mg Vial Label)

Label for Nalbuphine Hydrochloride Injection, 10 mg/mL, a multiple-dose solution for intravenous, intramuscular, or subcutaneous use. The label includes manufacturer Hospira, Inc., Lake Forest, IL, and instructions to protect from light and store at controlled room temperature. It specifies the presence of preservatives and buffers and notes it is sterile and nonpyrogenic.*

* 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.