Buprenorphine And Naloxone Tablet
Product Images NDC 72162-1347

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 72162-1347). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Chemical Structure (Buprenorphine 01)

Chemical structure of buprenorphine hydrochloride showing its molecular framework with labeled functional groups including hydroxyl, methoxy, and cyclopropyl moieties.*

FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical structure diagram of Buprenorphine, an active ingredient in the medication Buprenorphine and Naloxone. The diagram depicts the molecular structure including rings and functional groups characteristic of Buprenorphine hydrochloride dihydrate.*

FDA Label Image

Image (Buprenorphine 03)

An instructional illustration showing a person placing a sublingual tablet under the tongue, using the fingers to position the tablet correctly inside the mouth.*

FDA Label Image

Label (Lbl721621347)

Label for Buprenorphine and Naloxone Sublingual Tablets, USP, 8 mg/2 mg strength. The label indicates the product contains 30 tablets and is for sublingual administration. It is relabeled by Bryant Ranch Prepack and manufactured by Purdue Pharma L.P. The label includes NDC 72162-1347-3, storage instructions, and a warning to keep out of reach of children.*

* 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.