Buprenorphine Hcl Tablet
Product Images NDC 67296-2123

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hcl (NDC 67296-2123). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Chem-fig (Bup HCl Chem Fig)

Chemical structure of Buprenorphine HCl, showing its complex multi-ring structure with functional groups including hydroxyl, methoxy, and cyclopropylmethyl substitutions, alongside a hydrochloride (HCl) component.*

FDA Label Image

Ifu-image (Ifu Image)

An illustration showing a person placing a sublingual tablet under their tongue using their fingers. The image visually demonstrates the proper placement of a tablet for sublingual administration, relevant to products like Buprenorphine HCl sublingual tablets.*

FDA Label Image

Buprenorphine-sl-tabs-bl-2mg-c50000233-03-k02 (Image 01)

Label for Buprenorphine Sublingual Tablets 2 mg, containing 30 tablets. The label includes dosage strength, directions to see the package insert for complete prescribing information, storage conditions, and distributor information for Hikma Pharmaceuticals USA Inc. The label states prescription use only and includes a barcode.*

FDA Label Image

Buprenorphine-sl-tabs-bl-8mg-c50000232-02-k02 (Image 02)

Label for Buprenorphine Sublingual Tablets, 8 mg strength, in a 30-tablet package. The label includes dosage information, storage instructions, distribution by Hikma Pharmaceuticals USA Inc., and a barcode. The product is prescription only and features the Hikma logo.*

* 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.