Glimepiride Tablet
Product Images NDC 71921-216

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Glimepiride (NDC 71921-216). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Florida Pharmaceutical Products, Llc, 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

Glime Str (Glimestr)

Chemical structure of glimepiride, a sulfonylurea antidiabetic drug, showing its molecular arrangement including a urea, a sulfonyl group, and a cyclohexyl ring.*

FDA Label Image

Cart 1 mg (Fpp 1 mg)

Glimepiride Tablets USP 1 mg oral tablets label from Florida Pharmaceutical Products, LLC. The label indicates a quantity of 100 tablets with instructions 'Once a Day.' It includes dosage and administration instructions reference, storage conditions, and manufacturer information (Indoco Remedies Limited, India). The label shows NDC 71921-214-01 and includes barcodes.*

FDA Label Image

Cart 2 mg (Fpp 2 mg)

Glimepiride Tablets USP 2 mg oral tablet label. The label includes dosage strength of 2 mg, quantity of 100 tablets, NDC 71921-215-01, and notes Rx only status. It lists the manufacturer as Florida Pharmaceutical Products, LLC, Boca Raton, FL, and shows storage, warning, and pharmacist instructions. The label also displays barcodes and regulatory information.*

FDA Label Image

Cart 4 mg (Fpp 4 mg)

Glimepiride Tablets USP 4 mg oral tablets, packaged by Florida Pharmaceutical Products, LLC. The label indicates a 100-tablet count with dosage instructions to take once a day. It includes storage instructions, warnings, and manufacturer details, including Indoco Remedies Limited, India.*

FDA Label Image

Fpp (Fpp)

* 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.