Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 59651-549

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 59651-549). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (500 mg (100 Tablet Bottle))

Package Label-principal Display Panel (500 mg (100 Tablet Bottle))
Label for Metformin Hydrochloride Extended-Release Tablets USP, 500 mg, supplied by Aurobindo Pharma USA, Inc. It indicates 100 tablets per container, with storage instructions and a note to dispense in a light-resistant container. The label includes the NDC 59651-548-01 and specifies that the tablets are made in India.*
FDA Label Image

Package Label-principal Display Panel (750 mg (100 Tablet Bottle))

Package Label-principal Display Panel (750 mg (100 Tablet Bottle))
Label for Metformin Hydrochloride Extended-Release Tablets, USP 750 mg, distributed by Aurobindo Pharma USA, Inc. The label indicates 100 tablets per container and includes storage instructions and NDC 59651-549-01. The product is made in India by Aurobindo Pharma Limited.*
FDA Label Image

Structure (Metformin Str1)

Structure (Metformin Str1)
Chemical structure of Metformin Hydrochloride showing the molecular arrangement of atoms and bonds in the compound.*

* 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.