Glimepiride
Product Images NDC 0440-6566

3 FDA label images from Liberty Pharmaceuticals, Inc. · 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 0440-6566). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Liberty Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Structural Formula (Glimepiride Usp 4mg 1)

Structural Formula (Glimepiride Usp 4mg 1)
Chemical structure of the active ingredient Glimepiride, showing its molecular connectivity including a cyclohexyl group, sulfonylurea linkage, and amide functional groups as depicted in the structural formula diagram.*
FDA Label Image

Figure (Glimepiride Usp 4mg 2)

Figure (Glimepiride Usp 4mg 2)
Glimepiride 4 mg tablet packaging label from Liberty Pharmaceuticals, Inc. The box is primarily white with a blue and green design, indicating a 100-count supply. The product includes the proprietary name Glimepiride, strength of 4 mg, and the manufacturer's name and logo. The NDC 0440-6566 is also visible on the box.*
FDA Label Image

Image Label (Glimepiride Usp 4mg 3)

Image Label (Glimepiride Usp 4mg 3)
Label for Glimepiride 4 mg tablets by Liberty Pharmaceuticals, Inc. The label indicates this product is a generic for Amaryl and contains 100 tablets. It is packaged by Aidarex Pharmaceuticals LLC and manufactured by Carlsbad Technology Inc. The label includes storage instructions, prescription-only status, and tablet description (white round with CTI 117 on one side).*

* 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.