Buprenorphine Tablet
Product Images NDC 42858-501

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine (NDC 42858-501). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rhodes Pharmaceuticals 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

Chemical Structure (Buprenorphine 01)

Chemical structure diagram of buprenorphine hydrochloride, showing its molecular arrangement with functional groups and bonding pattern.*

FDA Label Image

Image (Buprenorphine 02)

An instructional black and white line drawing showing a person opening their mouth with a sublingual tablet being placed under the tongue on the lower jaw's gum area. One hand is positioning the tablet, demonstrating the correct method of sublingual tablet administration.*

FDA Label Image

Principal Display Panel (2 mg Tablet Bottle Label)

Label for Buprenorphine Sublingual Tablets, 2 mg strength, by Rhodes Pharmaceuticals LLC. The label includes dosage form and route (sublingual tablets), package size (30 tablets), and storage instructions (store at 20° to 25°C or 68° to 77°F). It also contains safety warnings for pharmacists and caregivers about accidental ingestion and child-resistant packaging.*

FDA Label Image

Principal Display Panel (8 mg Tablet Bottle Label)

Label for Buprenorphine Sublingual Tablets 8 mg by Rhodes Pharmaceuticals LLC. The label indicates the product is for prescription use, contains 30 tablets, and includes warnings for pharmacists and patient safety. The label also provides storage instructions and a barcode.*

* 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.