Buprenorphine And Naloxone Tablet
Product Images NDC 63629-9482

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 63629-9482). 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, including detailed rings and functional groups, displayed with a hydrochloride salt (HCl) notation.*
FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical Structure (Buprenorphine 02)
Chemical structure diagram of Buprenorphine hydrochloride dihydrate, showing its detailed molecular configuration including hydroxyl, ketone, and nitrogen groups along with associated chemical bonds.*
FDA Label Image

Image (Buprenorphine 03)

Image (Buprenorphine 03)
An instructional diagram showing a person opening their mouth and lifting their tongue with a finger, illustrating placement of a sublingual tablet under the tongue, relevant to the administration of Buprenorphine and Naloxone sublingual tablets.*
FDA Label Image

Label (Lbl636299482)

Label (Lbl636299482)
Label for Buprenorphine and Naloxone Sublingual Tablets, USP 2 mg/0.5 mg by Bryant Ranch Prepack. The label includes NDC 63629-9482-01 and indicates a package of 30 tablets. It also displays storage instructions and barcode with labeler 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.