Glimepiride
Product Images NDC 61919-723

3 FDA label images from Direct Rx · 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 61919-723). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

723-30 (723 30)

723-30 (723 30)
GLIMEPIRIDE 1 mg 30 tablets blister pack label. The label identifies the product as a generic for AMARYL, with each tablet containing Glimepiride USP 1 mg. The label includes lot number, expiration date, and NDC 61919-723-30, with labeling by Direct_Rx and storage instructions to keep out of reach of children and at 68-77 degrees Fahrenheit.*
FDA Label Image

723-90 (723 90)

723-90 (723 90)
Label for GLIMEPIRIDE 1 mg, packaged as 90 tablets. The label includes the generic reference to AMARYL and states each tablet contains Glimepiride USP 1 mg. It also shows the labeler as Direct_Rx and provides lot and expiration details, along with various regulatory and handling instructions.*
FDA Label Image

82be3a19 7f29 6822 E053 2a91aa0ac4ae

82be3a19 7f29 6822 E053 2a91aa0ac4ae
GLIMEPIRIDE 1 mg 30 tablets carton label from Direct_Rx, generic for AMARYL. The label shows the dosage strength, quantity, NDC 61919-723-30, and manufacturer information including lot and expiration date sections. The label includes storage instructions and usage warnings typical for prescription medication packaging.*

* 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.