Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 51224-007

View Photos of 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 Metformin Hydrochloride (NDC 51224-007). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tagi Pharma, 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 (Metformin 01)

Chemical Structure (Metformin 01)
Chemical structure diagram of Metformin Hydrochloride, showing the molecular arrangement including carbon, nitrogen, hydrogen atoms, and hydrochloride group associated with the active ingredient.*
FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Principal Display Panel (500 mg Tablet Bottle Label)
Label for Metformin Hydrochloride Extended-Release Tablets, USP, 500 mg strength, oral dosage form. The label indicates a package size of 1000 tablets and includes storage instructions, manufacturer information (CSPC Ouyi Pharmaceutical Co., Ltd.), and labeler TAGI Pharma, Inc. The NDC code 51224-007 is visible along with barcodes and logos for TAGI Pharma and CSPC.*
FDA Label Image

Principal Display Panel (750 mg Tablet Bottle Label)

Principal Display Panel (750 mg Tablet Bottle Label)
Label for Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, oral tablets. The label indicates 500 tablets per container, produced by TAGI Pharma, Inc., with manufacturing by CSPC Ouyi Pharmaceutical Co., Ltd. Storage instructions and pharmacist dispensing notes are included along with NDC 51224-107-60 and a barcode.*

* 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.