Buprenorphine And Naloxone Tablet
Product Images NDC 71335-2981

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 71335-2981). 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 (Buprenorphine 01)
Chemical structure of Buprenorphine and Naloxone hydrochloride (HCl) as depicted by the molecular diagram showing the arrangement of atoms, including hydroxyl (OH) groups and other functional groups characteristic of the compound.*
FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical Structure (Buprenorphine 02)
Chemical structure diagram of Buprenorphine Hydrochloride Dihydrate. The structure shows the molecular arrangement including rings and functional groups with the HCl and 2H2O notation indicating the hydrate form.*
FDA Label Image

Image (Buprenorphine 03)

Image (Buprenorphine 03)
An instructional illustration showing a person placing a tablet under the tongue, demonstrating the sublingual administration route typically used for Buprenorphine and Naloxone tablets.*
FDA Label Image

Label (Lbl713352981)

Label (Lbl713352981)
Label for Buprenorphine and Naloxone Sublingual Tablets, 8 mg/2 mg, with a quantity of 30 tablets. The label includes the NDC 71335-2981, indicates the tablets are Rx only, and shows the repackager Bryant Ranch Prepack and manufacturer Purdue Pharma L.P. Storage instructions recommend 20° to 25°C. There are QR codes for package insert and prescribing information.*

* 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.