Buprenorphine And Naloxone Tablet
Product Images NDC 72162-1346

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 72162-1346). 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, shown with labeled atoms and bonds, including functional groups and stereochemistry. The image highlights the complex molecular arrangement typical of this opioid partial agonist. A labeled hydrochloride (HCl) component is indicated as part of the structure.*

FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical structure diagram of Buprenorphine Hydrochloride Dihydrate, showing the molecular framework including hydroxyl, nitrogen, and ketone groups along with associated water and hydrochloride.*

FDA Label Image

Image (Buprenorphine 03)

An instructional illustration showing a person lifting their upper lip to place a sublingual tablet under the tongue. The diagram highlights the correct placement area for the tablet beneath the tongue, demonstrating proper administration technique for sublingual tablets.*

FDA Label Image

Label (Lbl721621346)

Label for Buprenorphine and Naloxone Sublingual Tablets, USP 2 mg/0.5 mg strength. The label shows the NDC 72162-1346-3 and specifies that the package contains 30 tablets. It includes storage instructions, pharmacy dosing guidance, and warnings about accidental ingestion by children. The product is relabeled by Bryant Ranch Prepack and manufactured by Purdue Pharma L.P.*

* 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.