Buprenorphine
Product Images NDC 67296-1506

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine (NDC 67296-1506). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, Inc., 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

Buprenorphine-label-2mg.jpg (Buprenorphine Label 2mg)

Label for Buprenorphine Sublingual Tablets 2 mg from Sun Pharma. The label highlights the strength as 2 mg and indicates the package contains 30 tablets. It includes a pharmacist instruction to dispense with a Medication Guide. The label also shows a barcode, lot number, and expiration date fields.*

FDA Label Image

Buprenorphine-label-8mg.jpg (Buprenorphine Label 8mg)

Buprenorphine Sublingual Tablets 8 mg carton label indicating prescription use with 30 tablets per package. The label features dispensing instructions for pharmacists to provide a Medication Guide with each patient. It includes a barcode, NDC 62756-460-83, and is labeled by Sun Pharma.*

FDA Label Image

Buprenorphine-figure (Buprenorphine Figure)

An instructional illustration showing the placement of a sublingual tablet under the tongue. The image depicts an open mouth with teeth, tongue, and throat, demonstrating the correct positioning for administering the medication.*

FDA Label Image

Buprenorphine-str (Buprenorphine Str)

Chemical structure diagram of Buprenorphine hydrochloride, showing its molecular components including hydroxyl, methoxy groups, and nitrogen-containing ring systems.*

* 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.