Buprenorphine Hcl Tablet
Product Images NDC 58118-0177

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

Label for Buprenorphine SL 2 mg Tablets, a sublingual tablet product by Clinical Solutions Wholesale, LLC. The label shows the NDC number 58118-0176-8, a quantity of 30 tablets, and indicates repackaging by Clinical Solutions Wholesale. It lists the manufacturer as Hikma Pharmaceuticals USA in Eatontown, NJ. The label includes batch and lot information fields and a QR code.*

FDA Label Image

Buprenorphine 8

Label for Buprenorphine SL 8 mg Tablets, sublingual tablets with a quantity of 30. The label includes the NDC 58118-0177-8 and indicates manufacturing by West-Ward Pharmaceuticals in Eatontown, NJ. Distributed by Clinical Solutions Wholesale, LLC with address in Franklin, TN. Additional information includes lot numbers, expiration date, barcodes, and usage instructions.*

FDA Label Image

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

Chemical structure diagram of Buprenorphine hydrochloride (Buprenorphine HCl), showing the molecular arrangement and presence of the HCl component.*

FDA Label Image

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

An illustration showing a person placing a sublingual tablet under the tongue using their fingers, demonstrating the route of administration for a sublingual 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.