Glimepiride Tablet
Product Images NDC 50268-360

4 FDA label images from Avpak · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Glimepiride (NDC 50268-360). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

358 (358 15)

358 (358 15)
Label for Glimepiride Tablets, USP 1 mg oral tablets by AvPAK. The label indicates a package of 50 tablets (5x10) with Rx only status and instructions for once daily use. It includes storage conditions, warnings, dosage reference to package insert, and manufacturer details for AvKARE, Inc., Pulaski, TN.*
FDA Label Image

359 (359 15)

359 (359 15)
Glimepiride Tablets, USP 2 mg oral tablets in a package of 50 tablets (5 x 10). The label includes dosage strength, barcode, manufacturer AvPAK for AvKARE, Inc., and storage instructions. The label states prescription use only and includes warnings and administration notes.*
FDA Label Image

360 (360 15)

360 (360 15)
Glimepiride Tablets USP 4 mg oral tablets packaging label. The label shows a carton containing 50 tablets (5 blisters of 10 tablets each) with a unit dose format, indicated for prescription use only (Rx only). Manufacturer information is AvPAK, a product of AvKARE, located in Pulaski, TN. The label includes dosage warnings, storage instructions, and barcodes for product identification.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Glimepiride, depicting its molecular connectivity and arrangement.*

* 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.