Buprenorphine Hcl
Product Images NDC 76519-1170

3 FDA label images from H.j. Harkins Company, Inc. · 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 Hcl (NDC 76519-1170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company, 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

Label (76519 1170 Scheduled Ppac Label)

Label (76519 1170 Scheduled Ppac Label)
Label for BUPRENORPHINE HCL SL 8MG tablets from H.J. Harkins Company, Inc. The label includes the proprietary name, strength (8MG), dosage form (tablet), and multiple instances of the product identification with NDC 76519-1170-XX, expiration date 00/00, lot number AB00CD, and manufacturer code 00054-0177-13. It contains a caution about federal law restricting drug transfer and dispensing, storage instructions, and a use directive stating 'Use As Directed by Physician.' The repackager information is noted at the bottom.*
FDA Label Image

Image 1 (Image 1)

Image 1 (Image 1)
An instructional illustration showing a person placing a buccal (sublingual) film or tablet inside the mouth, positioned near the lower gums or inner cheek. This demonstrates the administration method typical for sublingual or buccal drug delivery.*
FDA Label Image

Image (Image)

Image (Image)
Chemical structure diagram of buprenorphine hydrochloride showing its molecular framework with labeled functional groups including hydroxyl, methoxy, and tertiary butyl groups, along with the hydrochloride component.*

* 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.