Buprenorphine Tablet
Product Images NDC 0054-0176

4 FDA label images from Hikma Pharmaceuticals Usa Inc. · 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 (NDC 0054-0176). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., 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

Bup HCl Chem Fig

Bup HCl Chem Fig
Chemical structure of buprenorphine hydrochloride showing its molecular framework with rings, hydroxyl groups, methoxy groups, and a cyclopropylmethyl substituent.*
FDA Label Image

Ifu Image

Ifu Image
An instructional illustration showing a person placing a sublingual tablet under the tongue, demonstrating the correct administration method for sublingual tablets such as buprenorphine.*
FDA Label Image

Image 01

Image 01
Label for Buprenorphine Sublingual Tablets 2 mg by Hikma Pharmaceuticals USA Inc. The label shows a 30 tablet package. It mentions each tablet contains 2.16 mg of buprenorphine HCl USP equivalent to 2 mg buprenorphine base. Storage instructions note 20° to 25°C (68° to 77°F). The label includes dosing instructions to refer to the package insert and cautions for pharmacist dispensing and child safety.*
FDA Label Image

Image 02

Image 02
Label for Buprenorphine Sublingual Tablets 8 mg by Hikma Pharmaceuticals USA Inc., containing 30 tablets. The label includes dosage strength information, storage instructions, and a warning to dispense with an attached Medication Guide. The label also displays a barcode and the Rx only symbol.*

* 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.