Glimepiride
Product Images NDC 70934-232

2 FDA label images from Denton Pharma, Inc. Dba Northwind Pharmaceuticals · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Glimepiride (NDC 70934-232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Denton Pharma, Inc. Dba Northwind Pharmaceuticals, 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 (70934 232 30 Rev A 01 19)

Label (70934 232 30   Rev A 01 19)
Glimepiride Tablets USP 2 mg label containing 30 tablets, labeled Rx Only. The packaging shows dosage instructions to refer to the package insert, storage conditions at 25°C with allowed excursions to 20-25°C, and caution to keep out of reach of children. Manufactured and repackaged by Denton Pharma, Inc. DBA Northwind Pharmaceuticals, with barcode, NDC 70934-232-30, and additional manufacturing lot and expiration details.*
FDA Label Image

Structure (Glimepiride Structure)

Structure (Glimepiride Structure)
Chemical structure of Glimepiride active ingredient, showing its molecular components and arrangement with sulfonylurea and cyclohexyl 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.