Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 76385-129

3 FDA label images from Unichem Pharmaceuticals (usa), 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 76385-129). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Unichem Pharmaceuticals (usa), 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.

Product Images & Figures Index

FDA Label Image

Image (Image)

Image (Image)
Chemical structure of metformin hydrochloride, depicting the molecular arrangement including nitrogen, carbon, hydrogen atoms, and the hydrochloride component.*
FDA Label Image

500mg-1000-count-bottle-label (500mg 1000 Count Bottle Label)

500mg-1000-count-bottle-label (500mg 1000 Count Bottle Label)
Metformin Hydrochloride Extended-release Tablets, USP 500 mg tablet label by Sawgrass Pharma. The label indicates 1000 tablets in the package, manufactured by Beximco Pharmaceuticals PLC, Bangladesh, and distributed by Unichem Pharmaceuticals (USA), Inc. Storage instructions and NDC 76385-128-10 are present along with a barcode and Rx only designation.*
FDA Label Image

750mg-100-count-bottle-label (750mg 100 Count Bottle Label)

750mg-100-count-bottle-label (750mg 100 Count Bottle Label)
Metformin Hydrochloride Extended-release Tablets, USP 750 mg, oral tablet, extended release, in a package label showing 100 tablets. Manufactured by Beximco Pharmaceuticals PLC and distributed by Unichem Pharmaceuticals (USA), Inc., with storage instructions and NDC 76385-129-01 visible.*

* 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.