Buprenorphine Hydrochloride And Naloxone Hydrochloride Dihydrate Tablet
Product Images NDC 58118-0549

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 58118-0549). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, Llc, 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

Chemicalstructurebupren (Chemicalstructure1)

Chemical structure of buprenorphine hydrochloride, showing its molecular framework including rings, functional groups, and hydrochloride association as represented in the diagram.*

FDA Label Image

Chemicalstructurenal (Chemicalstructure2)

Chemical structure of Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate, depicted with molecular framework including functional groups and hydration. The structure includes labeled HCl and 2H2O indicating the hydrochloride salt and dihydrate form.*

FDA Label Image

Buprenorphine/naloxone 2/0.5mg Sl Tablet 30ct Blister Card (Containerlabel2mgpoint5mg)

Packaging label for Buprenorphine/Naloxone 2/0.5 mg sublingual tablets by Clinical Solutions Wholesale, LLC. The label shows the NDC 58118-0549, quantity of 30 tablets, and manufacturer Accord Healthcare, Inc. with a manufacturing lot number SAMPLE123 and expiration date March 2027.*

FDA Label Image

Figure1 (Fig1)

Illustration showing a person placing a tablet under their tongue, demonstrating the sublingual route of administration for a tablet dosage form.*

* 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.