Nalbuphine Hydrochloride Injection
Product Images NDC 71872-7331

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nalbuphine Hydrochloride (NDC 71872-7331). 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

7331.pdp (7331)

Nalbuphine Hydrochloride Injection 10 mg/mL in a 10 mL multiple-dose vial label. The label states usage for intramuscular, subcutaneous, or intravenous administration, with preservatives and stabilizers listed. It includes the lot number, expiration date, storage conditions, and repackaging information by Medical Purchasing Solutions, Scottsdale, AZ. The label also features a barcode and manufacturer details for Somerset Therapeutics, LLC.*

FDA Label Image

Image (D4c32b91 24cf 43f2 A1d2 0120f31bbba8 01)

Chemical structure diagram of Nalbuphine hydrochloride showing the molecular configuration with hydroxyl groups and a cyclobutyl group, including the HCl as part of the hydrochloride salt form.*

FDA Label Image

Nalb.pdp (Nalb)

Nalbuphine Hydrochloride Injection 100 mg/10 mL (10 mg/mL) multiple-dose vial label. The injection is for intramuscular, subcutaneous, or intravenous use. The label includes dosage form and strength, manufacturer Somerset Therapeutics, LLC, and storage instructions. It also notes preservatives and other inactive ingredients. Barcode and lot/expiration area instructions are visible.*

* 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.