Buprenorphine Tablet
Product Images NDC 0904-7155

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 (NDC 0904-7155). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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

Chem-fig (Bup HCl Chem Fig)

FDA Label Image

Ifu-image (Ifu Image)

FDA Label Image

Image 01

Image 01
This is a description of a medication named Buprenorphine, in the form of sublingual tablets, produced by Major Pharmaceuticals and distributed in unit doses. Each tablet contains 218mg of buprenorphine HC. The product comes as a prescription of 30 tablets with a medication guide. The recommended dosage of the medication is provided in the product insert and comes with precautions and warnings. The medication needs to be stored at 20-25C temperature according to US-controlled room temperature standards and should be kept out of reach of children. The text also includes the information of the pharmaceutical company that manufactures and distributes the medication.*
FDA Label Image

Image 02

Image 02
This is the information for the medication Buprenorphine Sublingual Tablets by Major Pharmaceuticals. The item has a NDC number of 0904-7155-04 and comes in a unit dose of 30 tablets. The tablets contain .64 mg of Buprenorphine HC, USP, equivalent 108 mg of bis. The recommended storage temperature is between 20° to 28°C (68° to 77°F). The medication guide is found on the manufacturer's website, and dispensed by a pharmacist. The text contains warnings based on ingestion by children accidentally.*

* 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.