Metformin Hydrochloride Tablet
Product Images NDC 70010-063

7 FDA label images from Granules Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 70010-063). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules 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.

FDA Label Image

Metformin-063-06.jpg.jpg (Metformin 063 06.jpg)

Metformin-063-06.jpg.jpg (Metformin 063 06.jpg)
Label for Metformin Hydrochloride Tablets, USP 500 mg, a prescription tablet by Granules Pharmaceuticals Inc. The label specifies 60 tablets per container and indicates storage instructions between 20° to 25° C with permitted excursions. Manufactured by Granules India Limited in Hyderabad, India. The label includes an NDC code, barcode, and space for lot and expiration information.*
FDA Label Image

Metformin-063-10.jpg.jpg (Metformin 063 10.jpg)

Metformin-063-10.jpg.jpg (Metformin 063 10.jpg)
Label for Metformin Hydrochloride Tablets USP 500 mg, bottle containing 1000 tablets. Manufactured by Granules India Limited, India, and labeled for Granules Pharmaceuticals Inc. The label includes storage instructions, dosage form, strength, and dispensing requirements. NDC 70010-063-10 is visible on the label.*
FDA Label Image

Metformin-064-06.jpg.jpg (Metformin 064 06.jpg)

Metformin-064-06.jpg.jpg (Metformin 064 06.jpg)
Label for Metformin Hydrochloride Tablets, USP 850 mg, manufactured for Granules Pharmaceuticals Inc. The label indicates a count of 60 tablets with prescription only status. Storage instructions specify controlled room temperature, and the label notes manufacturing by Granules India Limited in Hyderabad, India.*
FDA Label Image

Metformin-064-10.jpg.jpg (Metformin 064 10.jpg)

Metformin-064-10.jpg.jpg (Metformin 064 10.jpg)
Metformin Hydrochloride Tablets USP 850 mg label for a package of 1000 tablets. The label shows the active ingredient strength and highlights that it is Rx only. It includes storage instructions and manufacturer details for Granules Pharmaceuticals Inc., Chantilly, VA, with manufacturing by Granules India Limited. The label features a barcode and space for lot and expiration date printing.*
FDA Label Image

Metformin-065-06.jpg.jpg (Metformin 065 06.jpg)

Metformin-065-06.jpg.jpg (Metformin 065 06.jpg)
Metformin Hydrochloride Tablets USP 1000 mg, bottle label for 60 tablets. The label indicates the product is for Rx only and includes storage instructions, a barcode, and manufacturing details by Granules India Limited (Made in India) for Granules Pharmaceuticals Inc. Additional text notes usual dosage instructions and pharmacist dispensing information.*
FDA Label Image

Metformin-065-10.jpg.jpg (Metformin 065 10.jpg)

Metformin-065-10.jpg.jpg (Metformin 065 10.jpg)
Label for Metformin Hydrochloride Tablets, USP containing 1000 mg per tablet, manufactured by Granules Pharmaceuticals Inc. The label indicates a package of 1000 tablets, with storage instructions and pharmacist dispensing information. It is marked for prescription use only and identifies manufacturing in India by Granules India Limited.*
FDA Label Image

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

Metformin-structure.jpg.jpg (Metformin Structure.jpg)
Chemical structure of Metformin Hydrochloride showing its molecular arrangement including nitrogen, hydrogen, carbon atoms, and the hydrochloride group.*

* 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.