Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate Tablet
Product Images NDC 70518-3862

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 70518-3862). 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)

Label for buprenorphine hydrochloride and naloxone hydrochloride dihydrate sublingual tablets, strength 2 mg / 0.5 mg, package quantity 30 tablets. The label shows the Rx only status, NDC 70518-3862-00, and manufacturer as Hikma Pharma, Amman, Jordan. It includes a caution about federal law transfer restrictions and storage temperature guidelines. Labeler is RemedyRepack Inc.*

FDA Label Image

Buprenorphine-chem-structure.jpg (Image 02)

Chemical structure diagram of buprenorphine hydrochloride, showing its molecular arrangement with labeled atoms and bonds, including the HCl component.*

FDA Label Image

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

An instructional illustration showing the proper placement of a sublingual tablet under the tongue. The image depicts a hand holding a small tablet near an open mouth, highlighting the sublingual route of administration for the medication.*

FDA Label Image

Naloxone-chem-structure.jpg (Image 04)

Chemical structure diagram of buprenorphine hydrochloride and naloxone hydrochloride dihydrate, showing molecular bonds and atoms in a black line format on a white background.*

* 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.