Buprenorphine Hydrochloride Tablet
Product Images NDC 70518-4570

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Buprenorphine Hydrochloride (NDC 70518-4570). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm1 (Buprenorphine 2mg 70518 4570 00)

Label for Buprenorphine Sublingual Tablet C-II, 2 mg strength, with a quantity of 30 tablets per box. The label includes the NDC 70518-4570-00 and indicates that the product is repackaged by RemedyRepack Inc., Indiana, PA. Storage instructions and a caution regarding federal law on drug transfer are partially visible on the label.*

FDA Label Image

Remedy_label (Remedy Label)

Buprenorphine Sublingual Tablet C-III 2 mg, single tablet packaging from RemedyRepack Inc. The label includes dosage strength, quantity (1 tablet), NDC number 70518-4570-01, and important storage instructions. It also states federal transfer restrictions and contact information for the repackager in Indiana, PA.*

FDA Label Image

Ifu-image (Buprenorphine Sublingual Tablets Ifu Image)

An instructional line drawing illustrating the sublingual administration of a tablet. The image shows a hand placing a tablet under the tongue inside an open mouth, demonstrating the correct placement for sublingual absorption.*

FDA Label Image

"image Description" (Buprenorphine Sublingual Tablets Structure)

Chemical structure of buprenorphine hydrochloride, showing its molecular framework and 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.