Buprenorphine Hydrochloride
Product Images NDC 64725-1924

3 FDA label images from Tya Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride (NDC 64725-1924). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya 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

Label Image (64725 1924)

Label Image (64725 1924)
Label for buprenorphine hydrochloride sublingual tablets, 2 mg strength, repackaged by TYA Pharmaceuticals. The label shows a quantity of 30 tablets, a placeholder for lot number and expiration date, manufacturer listed as HI-TECH, and includes a barcode and contact information for T.Y.A. Pharmaceuticals in Tallahassee, FL.*
FDA Label Image

Chemical Structure (Buprenorphine Hydrochloride 1)

Chemical Structure (Buprenorphine Hydrochloride 1)
Chemical structure of buprenorphine hydrochloride, showing its molecular framework with hydroxyl, methoxy, and cyclopropyl groups, along with the hydrochloride salt indicated.*
FDA Label Image

Figure (Buprenorphine Hydrochloride 2)

Figure (Buprenorphine Hydrochloride 2)
An instructional line drawing showing the inside of an open mouth with a hand placing a round tablet on the lower gum near the teeth. This image visually demonstrates how to administer a sublingual or buccal tablet, relevant to buprenorphine hydrochloride use.*

* 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.