Metformin Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 68682-021

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 68682-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Oceanside Pharmaceuticals, 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

Chemical Structure-glumetza (76c50f01 B341 4046 A46e 712c40b5a4a0 01)

Chemical structure of metformin hydrochloride showing nitrogen, carbon, hydrogen atoms, and the hydrochloride component. The diagram details the molecular connectivity of the active ingredient metformin hydrochloride.*

FDA Label Image

Metformin500 (Carton Patheon)

Label of Oceanside Pharmaceuticals Metformin Hydrochloride Extended-Release Tablets 500 mg. The label indicates a dosage of once daily and contains 100 tablets. It includes warnings to keep out of reach of children, storage instructions, and a barcode. The NDC number is 68682-017-10.*

FDA Label Image

Tablets1000

Metformin hydrochloride extended-release tablets 1,000 mg label from Oceanside Pharmaceuticals. The label states the drug is for prescription only, to be taken once daily, with a package size of 90 tablets. It includes storage instructions and warnings, along with the NDC number 68682-018-90.*

FDA Label Image

Tablets500

Metformin Hydrochloride Extended-Release Tablets 500 mg label from Oceanside Pharmaceuticals. The label states the dosage strength of 500 mg and indicates a once-daily administration. The package contains 100 tablets. Additional information includes storage instructions, a barcode, NDC 68682-021-50, and handling details.*

* 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.