Buprenorphine Hcl Tablet
Product Images NDC 0406-7012

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hcl (NDC 0406-7012). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Specgx 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 HCl Sublingual Tabs 1)

Chemical structure of Buprenorphine Hydrochloride (Buprenorphine HCl) showing its molecular framework including aromatic rings and functional groups.*

FDA Label Image

Mouth Illustration (Buprenorphine HCl Sublingual Tabs 2)

An instructional diagram showing a person lifting their upper lip to expose the upper gum and teeth. A finger is pointing inside the mouth, likely illustrating application or placement of a sublingual tablet.*

FDA Label Image

Package Label Principal Display Panel (2 mg Tablets)

Label for Buprenorphine Sublingual Tablets 2 mg, containing 30 tablets. The label includes NDC 0406-7012-03, manufacturer SpecGx LLC (distributed by Mallinckrodt), and warnings about dispensing the medication guide. The label states the strength as 2 mg and shows a small image of a round tablet embossed with the number "2."*

FDA Label Image

Package Label Principal Display Panel (8 mg Tablet)

Label for Buprenorphine Sublingual Tablets 8 mg by SpecGx LLC, containing 30 tablets. The label highlights the strength as 8 mg and includes directions for pharmacists to dispense the medication guide. It also displays storage instructions and a barcode, along with a small image of a round white tablet embossed with the number "8."*

* 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.