Buprenorphine And Naloxone Tablet
Product Images NDC 71335-2828

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 71335-2828). 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 diagram of Buprenorphine and Naloxone showing the molecular framework with labeled functional groups, including hydroxyl and methoxy substituents, and an attached hydrochloride (HCl) component.*
FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical Structure (Buprenorphine 02)
Chemical structure diagram of Buprenorphine hydrochloride dihydrate, showing the molecular framework with hydroxyl, carbonyl, nitrogen, and aromatic components labeled.*
FDA Label Image

Image (Buprenorphine 03)

Image (Buprenorphine 03)
An instructional illustration showing a person lifting their upper lip to expose the gums above the upper front teeth, demonstrating where to place a sublingual tablet for Buprenorphine and Naloxone administration.*
FDA Label Image

Label (Lbl713352828)

Label (Lbl713352828)
Label for Buprenorphine and Naloxone 8 mg/2 mg sublingual tablets, USP by Bryant Ranch Prepack, relabeled by Bryant Ranch Prepack, Inc., manufactured by Purdue Pharma L.P. The label indicates a package of 30 tablets with NDC 71335-2828-1, including storage instructions and identification details embossed on the tablets.*

* 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.