Glimepiride Tablet
Product Images NDC 68001-586

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Glimepiride (NDC 68001-586). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

1mg Label (Glimepride 1mgmicrolabel)

Label for Glimepiride 1 mg tablets, USP, manufactured by BluePoint Laboratories. The label indicates a dosage form of oral tablets with a bottle count of 100 tablets. It includes NDC 68001-584-00, usage instructions to take once a day, and manufacturer details of Micro Labs Limited, Goa, India. Additional storage and warning information are present, along with barcodes.*

FDA Label Image

2 mg Label (Glimepride 2mgmicrolabel)

Glimepiride Tablets USP 2 mg oral tablets label by BluePoint Laboratories. The label indicates the product is prescription-only, with instructions to take once a day. It shows storage conditions and includes NDC 68001-585-00. The package contains 100 tablets and is manufactured by Micro Labs Limited, Goa, India for BluePoint Laboratories.*

FDA Label Image

4mg Label (Glimepride 4mgmicrolabel)

Glimepiride Tablets, USP 4 mg oral tablets by BluePoint Laboratories, shown in a package label. The label contains dosage information, warnings, and storage instructions. The package includes 100 tablets and is marked Rx Only. The label also features barcodes and manufacturing details.*

FDA Label Image

Structure (Glimepride Strc)

Chemical structure diagram of glimepiride, showing its molecular arrangement including a sulfonylurea group attached to a cyclohexyl ring and other functional groups.*

* 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.