C (Metformin Hydrochloride Extended Release Tablets 1)
Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 65162-179
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 65162-179). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Amneal Pharmaceuticals Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
A (Metformin Hydrochloride Extended Release Tablets 2)
This is a description of a medication that is Metformin Hydrochloride Extended-release Tablets, USP. Each tablet contains 500mg of Metformin Hydrochloride, and usual dosage instructions can be found in the enclosed package insert. The tablets should be stored in a tight, light-resistant container at a temperature between 20" to 25°C. The manufacturer is Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India, and it is distributed by Amneal Pharmaceuticals LLC in Bridgewater, NJ. The NDC number is 65162-178-10.*
B (Metformin Hydrochloride Extended Release Tablets 3)
The text describes Metformin Hydrochloride extended-release tablets, used for treating type 2 diabetes. The tablets come in a tight and light-resistant packaging along with a patient information leaflet. The usual dosage is mentioned in an enclosed package insert. The tablets should be stored at a temperature between 20°C to 25°C, and excursions are permitted between 15°C to 30°C. The tablets are manufactured by Amneal Pharmaceuticals located in Ahmedabad, India, and distributed by Amneal Pharmaceuticals LLC located in Bridgewater, NJ. No further information is available from the given text.*
* 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.
