Chem-fig (Bup HCl Chem Fig)
Chemical structure of buprenorphine hydrochloride showing its molecular bonds and chemical groups in a detailed illustration.*
Buprenorphine Tablet
Product Images NDC 0904-7154
4 FDA label images from Major Pharmaceuticals · 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 0904-7154). 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.
Ifu-image (Ifu Image)
An illustration showing a person placing a sublingual tablet under their tongue, demonstrating the proper administration method for sublingual tablets such as Buprenorphine.*
2mg Carton Label (E59c3c4f A9cc 412b B001 B9e430f537c5 01)
Label for Buprenorphine Sublingual Tablets 2 mg by Major Pharmaceuticals. The label indicates it is a unit dose package containing 30 tablets (3 x 10). It includes warnings for pharmacists and medication guides, dosage information, storage conditions, and distributor details for Major Pharmaceuticals, Indianapolis, IN. The label features an NDC code 0904-7154-04 and a barcode.*
8mg Carton Label (E59c3c4f A9cc 412b B001 B9e430f537c5 00)
Label for Major Pharmaceuticals Buprenorphine 8 mg sublingual tablets in a unit dose package. The label includes the NDC number 0904-7155-04, states the package contains 30 tablets (3 x 10), and notes the tablets contain buprenorphine HCl equivalent to 8 mg base. It includes pharmacist dispensing instructions, storage conditions, child safety warnings, revision date 09/24, and distributor information with a barcode at the bottom.*
* 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.
