Glimepiride Tablet
Product Images NDC 68084-326

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Glimepiride (NDC 68084-326). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

Ahp78825

Glimepiride 2 mg oral tablet shown with an oblong shape and reddish color. One side is imprinted with 'RDY' and the other side with '3 | 20'. This tablet is part of the American Health Packaging label set for Glimepiride in varying strengths.*

FDA Label Image

Ahp32601

Glimepiride 2 mg oral tablet, oval and green, imprinted with "RDY" on one side and "3 | 21" divided by a score line on the other side. Manufactured by American Health Packaging.*

FDA Label Image

Ahp32701

Glimepiride 2 mg oral tablet, blue, oval-shaped with imprint "RDY" on one side and "3 22" on the other side. This medication is manufactured by American Health Packaging.*

FDA Label Image

Structural Formula (Structure)

Chemical structure of glimepiride, a sulfonylurea class antidiabetic medication. The diagram shows the molecular connections including a cyclohexyl group, a sulfonylurea moiety, and a pyrrole ring with attached methyl groups.*

FDA Label Image

1 mg Glimepiride Tablets Carton (1 mg Glimepiride Tablets Carton)

Label for Glimepiride 1 mg tablets, USP by American Health Packaging. The label indicates a 30-tablet count (5x6) for oral use, with a green gradient background behind the strength. It includes storage instructions, protection warnings, NDC 68084-788-25, and distribution information for American Health Packaging, Columbus, Ohio. A QR code for current prescribing information is also visible.*

FDA Label Image

1 mg Glimepiride Tablet Blister (1 mg Blister)

Packaging label for Glimepiride tablet, USP 1 mg, oral tablet in a human prescription drug format. The label indicates the dosage strength of 1 mg and states 'ONCE A DAY'. It includes lot number and expiry date fields, a barcode, and is labeled by American Health Packaging, Columbiana, OH 44427. The label appears in three perforated sections, each identical.*

FDA Label Image

2 mg Glimepiride Tablets Carton (2 mg Glimepiride Tablets Carton)

Glimepiride 2 mg oral tablets, USP, packaged as 100 tablets (10 blister packs of 10 tablets each). The label indicates once daily dosing and is distributed by American Health Packaging in Columbus, Ohio. The NDC is 68084-326-01.*

FDA Label Image

2 mg Glimepiride Tablet Blister (2 mg Blister)

Sheet of multiple Glimepiride 2 mg tablets packaging labels, each marked as once a day oral tablets. Labels feature dosage strength (2 mg), drug name, UPC barcode, lot number, expiration date, and American Health Packaging as the labeler, located in Columbus, Ohio.*

FDA Label Image

4 mg Glimepiride Tablets Carton (4 mg Glimepiride Tablets Carton)

Glimepiride 4 mg tablets, USP, oral use, supplied in a bottle or carton containing 100 tablets (10 x 10). The label indicates the medication is for once a day use and is Rx only. It is manufactured and distributed by American Health Packaging. The label includes the NDC number 68084-327-01 and storage instructions.*

FDA Label Image

4 mg Glimepiride Tablet Blister (4 mg Blister)

Glimepiride 4 mg oral tablets from American Health Packaging. The label states the product is a Human Prescription Drug, taken once a day. Each label includes the lot number 123456 and expiration date 02/16, along with barcodes and manufacturing details for Columbia, OH.*

* 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.