Glimepiride
Product Images NDC 10544-219

View Photos of 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 Glimepiride (NDC 10544-219). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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 2mg 30ct (Label Glimepiride Tabs 2mg Bpi(10544 217 30) Dr Reddys(55111 321 05) Rev2)

Label 2mg 30ct (Label Glimepiride Tabs 2mg Bpi(10544 217 30) Dr Reddys(55111 321 05) Rev2)
Label for Glimepiride Tablets USP, 2mg, by Blenheim Pharmacal, Inc. The label indicates a package of 30 tablets, Rx only. Storage instructions specify controlled room temperature 20°-25°C and a tight, light-resistant container. NDC number 10544-217-30 and manufacturer code 55111-321-05 are shown, with placeholder lot and expiration dates.*
FDA Label Image

Label 4mg 30ct (Label Glimepiride Tabs 4mg Bpi(10544 219 30) Dr Reddys(55111 322 05) Rev2)

Label 4mg 30ct (Label Glimepiride Tabs 4mg Bpi(10544 219 30) Dr Reddys(55111 322 05) Rev2)
Label for Glimepiride Tablets, USP 4 mg, containing 30 tablets. The label specifies Rx Only and includes storage instructions for controlled room temperature. Manufacturer information lists Blenheim Pharmacal, Inc. with NDC 10544-219-30 and MFG code 55111-322-05. Additional details include package lot number, expiry date placeholders, and barcode.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of the active ingredient Glimepiride, showing its molecular framework with labeled atoms and bonds.*

* 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.