Buprenorphine And Naloxone Tablet
Product Images NDC 63629-9483

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 63629-9483). 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, showing its complex fused ring system, functional groups including hydroxyl, methoxy, and a cyclopropylmethyl substitution, represented with standard chemical notation. The image also indicates the presence of hydrochloride (HCl) salt form.*

FDA Label Image

Chemical Structure (Buprenorphine 02)

Chemical structure diagram of the active ingredient Buprenorphine hydrochloride dihydrate, showing its molecular framework including hydroxyl, carbonyl, and amine groups, as well as the hydrochloride and water of crystallization (HCl · 2H2O) components.*

FDA Label Image

Image (Buprenorphine 03)

An instructional illustration showing a person placing a tablet under the tongue, demonstrating the sublingual administration route for a medication.*

FDA Label Image

Label (Lbl636299483)

Label for Buprenorphine and Naloxone Sublingual Tablets, USP with a strength of 8 mg/2 mg. The label includes the NDC number 63629-9483-01 and indicates the product is supplied by Bryant Ranch Prepack. The package contains 30 tablets and is for prescription use only. Storage instructions and warnings for patient safety are also present.*

* 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.