Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 70518-4710

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 70518-4710). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack 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

Mm1 (Metformin HCl 1000mg 70518 4710 00)

Mm1 (Metformin HCl 1000mg 70518 4710 00)
Metformin Hydrochloride 1000 mg extended-release tablets packaging label showing a quantity of 50 tablets per box. Label states the product is repackaged by RemedyRepack Inc., Indiana, PA. The label includes warnings about not breaking, crushing or chewing tablets, storage instructions, and manufacturer information for Aurobindo Pharma, Hyderabad, India.*
FDA Label Image

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Metformin Hydrochloride extended-release tablet 1000 mg in a single tablet quantity. The label identifies the manufacturer as RemedyRepack Inc., Indiana, PA. The National Drug Code (NDC) on the label is 70518-4710-01. The tablet is described as round and white with imprint MTN1000. The label includes storage instructions and warnings against crushing or chewing the tablet.*
FDA Label Image

Structure (Metformin Str)

Structure (Metformin Str)
Chemical structure diagram of Metformin Hydrochloride showing the molecular arrangement of atoms, including nitrogen, carbon, hydrogen, and associated hydrochloride.*

* 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.