Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 68180-338

3 FDA label images from Lupin Pharmaceuticals, Inc. · 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 68180-338). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

Image-01 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 01)

Image-01 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 01)
Chemical structure of metformin hydrochloride showing its molecular arrangement with two methyl groups and multiple nitrogen atoms connected by carbon and nitrogen bonds, labeled with HCl indicating the hydrochloride form.*
FDA Label Image

Image-02 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 02)

Image-02 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 02)
Label for Metformin Hydrochloride Extended-Release Tablets USP 500 mg by Lupin Pharmaceuticals, Inc. The oral tablet package contains 100 extended-release tablets. Label includes dosage strength, storage instructions, and manufacturer details, with a note to see the package insert for prescribing information.*
FDA Label Image

Image-03 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 03)

Image-03 (F7e712aa B1bf 4ecd 8d72 2b1cb68611ce 03)
Label for Metformin Hydrochloride Extended-Release Tablets USP 1000 mg, oral extended-release tablets. The label shows the NDC 68180-339-09 and indicates a quantity of 90 tablets. It includes dispensing instructions, storage conditions, and manufacturer details: Lupin Pharmaceuticals, Inc. in Baltimore, Maryland, and Lupin Limited in Goa, India.*

* 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.