Buprenorphine Hydrochloride Tablet
Product Images NDC 50090-7559

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride (NDC 50090-7559). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Chemical Structure (Buprenorphine Hydrochloride 1)

Chemical Structure (Buprenorphine Hydrochloride 1)
Chemical structure of buprenorphine hydrochloride, showing its molecular framework with multiple rings, hydroxyl, methoxy groups, and a cyclopropylmethyl substituent, representing the active ingredient's detailed composition.*
FDA Label Image

Figure (Buprenorphine Hydrochloride 2)

Figure (Buprenorphine Hydrochloride 2)
An instructional black-and-white illustration showing a hand placing a sublingual tablet under the tongue of an open mouth. This image demonstrates the proper administration route for a sublingual tablet, likely for buprenorphine hydrochloride.*
FDA Label Image

Label Image (Lbl500907559)

Label Image (Lbl500907559)
Label for buprenorphine hydrochloride sublingual tablets, 8 mg strength, marketed by A-S Medication Solutions. The label indicates each tablet contains 8.64 mg buprenorphine HCl equivalent to 8 mg buprenorphine. Packaging contains 30 tablets with storage instructions to keep at 40 to 70 degrees Fahrenheit. Includes distributor information and a note to see package insert for dosing.*

* 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.