Buprenorphine Hcl Tablet
Product Images NDC 58118-0177

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 Hcl (NDC 58118-0177). 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

Buprenorphine 2

Buprenorphine 2
Clinical Solutions Wholesale is a company based in Franklin, TN, USA that repacked and/or distributed uprenorphine SL 2mg Tablets by Hikma Pharmaceuticals USA with Lot #: SAMPLE123 Batch #: SAMPLE456 and an expiration date of 2021 Jul. The product has a National Drug Code (NDC) number of 00054-0176-13 and a Global Trade Item Number (GTIN) of 0035811801768. The product comes in a package of 30 tablets with a Drug Code (DC) of 58118-0176-8. The location of the manufacturer is in Eatontown, NJ, USA, 07724.*
FDA Label Image

Buprenorphine 8

Buprenorphine 8
This is a label for a medication called Buprenorphine SL 8mg Tablets, with the NDC code 58118-0177-8 and 30 tablets in the package. There is also information about Mig, with the NDC code 00054-0177-13, lot number SAVPLET23, batch number SAMPLE4S6, and expiration date of July 2021. The medication was manufactured by West-Ward Pharmaceuticals in Eatontown, NJ, and repackaged/distributed by Clinical Solutions Wholesale in Franklin, TN.*
FDA Label Image

Buprenorphine-hcl-chem-figure.jpg (Buprenorphine HCl Chem Figure)

FDA Label Image

Buprenorphine-medguide-graphic.jpg (Buprenorphine Medguide Graphic)

* 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.