Metformin Hydrochloride Tablet, Coated
Product Images NDC 69367-382

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 69367-382). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Metformin 01)

Chemical Structure (Metformin 01)
Chemical structure of Metformin Hydrochloride, showing its molecular composition with methyl groups, nitrogen atoms, and the hydrochloride component.*
FDA Label Image

Principal Display Panel (500 mg Tablet Bottle Label)

Principal Display Panel (500 mg Tablet Bottle Label)
Label for Metformin Hydrochloride Tablets USP 500 mg, oral coated tablets. The label indicates a package size of 1000 tablets, manufactured for Westminster Pharmaceuticals, LLC and produced by CSPC Ouyi Pharmaceutical Co., Ltd. Storage instructions and barcode are also featured.*
FDA Label Image

Principal Display Panel (850 mg Tablet Bottle Label)

Principal Display Panel (850 mg Tablet Bottle Label)
Label for Metformin Hydrochloride Tablets, USP 850 mg coated tablets, packaged as 1000 tablets. Label includes storage instructions, manufacturer CSPC Ouyi Pharmaceutical Co., Ltd., and the labeler Westminster Pharmaceuticals, LLC. NDC code 69367-382-10 is displayed along with a barcode and other regulatory information.*
FDA Label Image

Principal Display Panel (1000 mg Tablet Bottle Label)

Principal Display Panel (1000 mg Tablet Bottle Label)
Label for Metformin Hydrochloride Tablets, USP 1000 mg, oral coated tablets, 1000 count. The label includes storage instructions, manufacturer details (CSPC Ouyi Pharmaceutical Co., Ltd., China), and the labeler Westminster Pharmaceuticals, LLC, Nashville, TN. The NDC is 69367-383-10.*

* 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.