Glumetza Tablet, Film Coated, Extended Release
Product Images NDC 68012-002

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Glumetza (NDC 68012-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Santarus, 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.

FDA Label Image

Chemical Structure-glumetza (Structural Formula)

Chemical structure diagram of metformin hydrochloride, the active ingredient in Glumetza, showing its molecular components and bonds.*

FDA Label Image

A Black Text On A White Background Ai-generated Content May Be Incorrect. (Image 03)

FDA Label Image

Pdp2 (Image 01)

Packaging label for Glumetza 500 mg extended-release tablets, oral use, with 100 tablets per package. The label includes NDC 68012-004-50, indicates prescription use only, and lists Santarus, Inc. as the labeler. The design features blue and white colors with dosing instructions "Once Daily."*

FDA Label Image

Carton2.jpg (Baf4bb5f 922f 4478 B7e0 4698f4a17cd0 01)

Glumetza 500 mg extended-release tablets (metformin hydrochloride) film-coated oral tablets by Santarus, Inc. The label indicates a 100-tablet count, once daily dosage, and includes the NDC 68012-002-13 and Rx only status. The label also shows regulatory information and a barcode.*

FDA Label Image

Pdp1 (Image 02)

Label for Glumetza 1,000 mg extended-release tablets (metformin hydrochloride), an oral prescription drug. The label indicates a 90-count tablet bottle for once-daily dosing. It includes the NDC 68012-003-16 and the Salix Pharmaceuticals logo, along with storage and safety warnings.*

* 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.