Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 68180-337

3 FDA label images from Lupin Pharmaceuticals, 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 68180-337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lupin Pharmaceuticals, 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

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B1f41565 1833 4dac 868b D7ff80c378c6 01
Chemical structure of Metformin Hydrochloride, showing the molecular arrangement of atoms and bonds characteristic of this active pharmaceutical ingredient.*
FDA Label Image

B1f41565 1833 4dac 868b D7ff80c378c6 02

B1f41565 1833 4dac 868b D7ff80c378c6 02
Label for Metformin Hydrochloride Extended-release Tablets USP 500 mg by Lupin Pharmaceuticals, Inc. The label shows 60 coated extended-release oral tablets per container. It includes storage instructions, dosage guidance to see package insert, and manufacturing details for Lupin Pharmaceuticals, Baltimore, Maryland, and Lupin Limited, India.*
FDA Label Image

B1f41565 1833 4dac 868b D7ff80c378c6 03

B1f41565 1833 4dac 868b D7ff80c378c6 03
Metformin Hydrochloride Extended-release Tablets USP 1000 mg oral tablets label from Lupin Pharmaceuticals, Inc. The label indicates 60 coated extended-release tablets per container with storage instructions and manufacturer information for Lupin Pharmaceuticals, Inc. (Baltimore, Maryland) and Lupin Limited (Goa, India). The label includes dosage, pharmacist dispensing guidance, and safety warnings.*

* 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.