Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate Tablet
Product Images NDC 71335-1720

4 FDA label images from Bryant Ranch Prepack · 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 71335-1720). 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 diagram of buprenorphine hydrochloride, depicting its molecular framework including rings, hydroxy, methyl, and methoxy groups, accompanied by the hydrochloride (HCl) component.*
FDA Label Image

Image 03

Image 03
An illustration showing a hand placing a sublingual tablet under the tongue inside an open mouth. The image demonstrates the sublingual route of administration for a tablet dosage form, relevant to buprenorphine hydrochloride and naloxone hydrochloride dihydrate tablets.*
FDA Label Image

Image 04

Image 04
Chemical structure of buprenorphine hydrochloride and naloxone hydrochloride dihydrate showing the molecular arrangement with rings, hydroxyl group, nitrogen atom, and associated hydrochloride and water molecules.*
FDA Label Image

Label (Lbl713351720)

Label (Lbl713351720)
Label for buprenorphine hydrochloride and naloxone hydrochloride dihydrate 2 mg/0.5 mg sublingual tablets. The label indicates it is packaged by Bryant Ranch Prepack in Burbank, CA. It includes a comparison to Suboxone 2 mg/0.5 mg tablets and a package size of 30 tablets. Storage instructions specify room temperature 20°-25°C (68°-77°F), and a note to keep out of reach of children. The NDC is 71335-1720-1.*

* 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.