Glyburide Tablet
Product Images NDC 62135-585

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Glyburide (NDC 62135-585). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Chartwell Rx, 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

Buprenorphine Sublingual Tablets 2 mg (NDC 72888-182-30)

GlyBURIDE Tablets, USP 1.25 mg oral tablets in a bottle of 30 tablets. The label is for a prescription drug manufactured by Chartwell RX, LLC, with storage instructions and a UPS controlled room temperature specification. The label also includes a barcode and batch information, with a note indicating no varnish on the label.*

FDA Label Image

Buprenorphine Sublingual Tablets 2 mg (NDC 72888-182-90)

Label for GlyBURIDE 2.5 mg tablets, USP, oral tablet prescription drug. The label indicates 30 tablets in the package, manufactured by Chartwell Rx, LLC. Storage instructions and other regulatory information are also printed alongside a barcode and an orange vertical text noting 'No Varnish.'*

FDA Label Image

Buprenorphine Sublingual Tablets 8 mg (NDC 72888-183-30)

Glyburide Tablets, USP 5 mg oral tablets label from Chartwell Rx, LLC. The label indicates prescription use only with a quantity of 90 tablets. It includes storage instructions and cautions to keep the product out of reach of children. The label also features the NDC number 62135-585-90 and a barcode.*

FDA Label Image

Image Description (Glyburide Tablets Structure)

Chemical structure diagram of Glyburide showing its molecular components and bonds, including a chlorinated aromatic ring, methoxy group, sulfonylurea linkage, and cyclohexyl group.*

* 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.