Buprenorphine And Naloxone Film
Product Images NDC 67296-2063

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Buprenorphine And Naloxone (NDC 67296-2063). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Buprenorphine And Naloxone Sublingual Film 2 mg/0.5 mg Carton Label (Image 01)

Packaging label for Buprenorphine and Naloxone Sublingual Film 2 mg/0.5 mg by Mylan Pharmaceuticals Inc. The label shows a blue and white carton design with green and black text, indicating 30 pouches each containing 1 sublingual film. The label includes directions for administration, storage instructions, and a barcode.*

FDA Label Image

Buprenorphine And Naloxone Sublingual Film 4 mg/1 mg Carton Label (Image 02)

Packaging label for Buprenorphine and Naloxone Sublingual Film 4 mg/1 mg by Mylan Pharmaceuticals Inc. The label features drug name, strength, dosage form, and usage warnings. It indicates a 30-pouch carton, each pouch containing one sublingual film. Storage instructions, administration guidelines, and distributor details are also shown.*

FDA Label Image

Buprenorphine And Naloxone Sublingual Film 8 mg/2 mg Carton Label (Image 03)

Packaging label for Buprenorphine and Naloxone Sublingual Film 8 mg/2 mg by Mylan Pharmaceuticals. The label shows the product name, strength, dosage form, and route (sublingual). The box has instructions for use, storage, and warnings about accidental ingestion by children. It indicates a package count of 30 pouches, each containing one sublingual film, and includes barcodes and the Mylan logo.*

FDA Label Image

Buprenorphine And Naloxone Sublingual Film 12 mg/3 mg Carton Label (Image 04)

Packaging label for Buprenorphine and Naloxone Sublingual Film, 12 mg/3 mg strength. The label shows that the product contains 30 pouches, each with one sublingual film, and is marked Rx only. Manufactured by Mylan Pharmaceuticals Inc. The label includes usage instructions and safety warnings, along with barcode and NDC 0378-8768-93.*

FDA Label Image

Buprenorphine Hydrochloride Structrual Formula (Image 05)

Chemical structure of Buprenorphine hydrochloride, depicted as a molecular diagram showing its cyclic and functional groups in black lines with an HCl component indicated on the right side.*

FDA Label Image

Naloxone Hydrochloride Structural Formula (Image 06)

Chemical structure of Buprenorphine Hydrochloride Dihydrate, identified by its complex ring system, hydroxyl groups, and molecular connectivity as depicted in the structural formula.*

FDA Label Image

Instructions For Use Figure 1 (Image 07)

An instructional illustration depicting hands using scissors to cut along a dotted line on a strip of packaging containing a buccal or sublingual film. The image shows how to open the packaging by cutting it to access the film dose inside.*

FDA Label Image

Instructions For Use Figure 2 (Image 08)

An instructional illustration showing a buccal or sublingual film placed inside an open mouth, positioned on the inner cheek or under the tongue, demonstrating the administration route for buccal or sublingual film dosage forms.*

FDA Label Image

Instructions For Use Figure 3 (Image 09)

Illustration showing the proper placement of a buccal or sublingual film inside the mouth. One image depicts placing the film inside the lower lip against the gums (buccal placement), and the other shows the film placed under the tongue (sublingual placement).*

* 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.