Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate Tablet
Product Images NDC 71335-1653

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 Hydrochloride And Naloxone Hydrochloride Dihydrate (NDC 71335-1653). 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.

Product Images & Figures Index

FDA Label Image

Image 02

Image 02
Chemical structure of buprenorphine hydrochloride, depicting its molecular framework with rings, hydroxyl groups, and a hydrochloride moiety, consistent with the active ingredient in the labeled product.*
FDA Label Image

Image 03

Image 03
An instructional illustration showing a person placing a sublingual tablet under their tongue. The image highlights the oral cavity with the lips parted and a hand holding the tablet near the lower teeth for sublingual administration.*
FDA Label Image

Image 04

Image 04
Chemical structure diagram of buprenorphine hydrochloride and naloxone hydrochloride dihydrate, showing molecular connectivity and associated hydrochloride and water of hydration groups.*
FDA Label Image

Label Image (Lbl713351653)

Label Image (Lbl713351653)
Label of buprenorphine hydrochloride and naloxone hydrochloride dihydrate 2 mg/0.5 mg sublingual tablets, packaged by Bryant Ranch Prepack in Burbank, CA. The label compares the product to Suboxone SL 2/0.5 mg tablets, includes storage instructions at 20-25°C (68-77°F), and a caution to keep out of reach of children. The package contains 30 tablets and shows the NDC 71335-1653-1.*

* 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.