Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate Tablet
Product Images NDC 70518-3844

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate (NDC 70518-3844). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Remedy_label (Remedy Label)

Packaging label for buprenorphine hydrochloride and naloxone hydrochloride dihydrate sublingual tablets, 8 mg / 2 mg strength, containing 30 tablets. The label shows the proprietary name, dosage form, quantity, and indicates it is a Schedule III drug. It is repackaged by RemedyRepack Inc., with manufacturing credited to Hikma Pharma in Amman, Jordan. The label includes a barcode, QR code, and directions to see the package insert.*

FDA Label Image

Buprenorphine-chem-structure.jpg (Image 02)

Chemical structure of buprenorphine hydrochloride showing the molecular arrangement of atoms and bonds, including the hydrochloride component.*

FDA Label Image

Bupr-naloxone-ifu-mouth-image (Image 03)

An instructional illustration showing a hand placing a tablet under the tongue inside an open mouth. The image visually demonstrates the sublingual route of administration for a tablet, likely representing how to take buprenorphine hydrochloride and naloxone hydrochloride dihydrate sublingual tablets.*

FDA Label Image

Naloxone-chem-structure.jpg (Image 04)

Chemical structure of buprenorphine hydrochloride dihydrate, showing its molecular rings, hydroxyl group, and side chain, with notation for hydrochloride and two 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.