Metformin Hydrochloride Tablet
Product Images NDC 70518-3084

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 70518-3084). 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

Remedy_label (Remedy Label)

This is a medication called metFORMIN HCI in the form of a tablet with a strength of 850 mg. It comes in a package of 30 tablets and is only available through prescription (RX only). The package has an NDC # of 70518-3084-00 and has a LOT # and expiration date printed on it. The medication should be stored at a temperature of 20-25°C (B-77°F) but can tolerate excursions up to 15-30°C (59-26°F). The manufacturer of the medication is Granules and it was packaged by RemedyRepack Inc. It is recommended to keep this medication and all other medications out of reach of children.*

FDA Label Image

Metformin HCl 850mg 70518 3084 01

This is a prescription medication called metformin HCI in tablet form with a strength of 850 mg. The National Drug Code (NDC) is 70518-3084-01 and the medication has been repackaged by RemedyRepack Inc. The manufacturing location is Granules in Chartilly, VA, and the source NDC is 70010-0064-10. The medication should be kept away from children and stored between 20-25°C (B-77°F); excursions permitted in 15-30°C (59-86°F). The expiration date and lot number are not available. The package insert should be referred to for usage instructions.*

FDA Label Image

Metformin-structure.jpg.jpg (Metformin Structure.jpg)

* 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.