Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 72789-106

3 FDA label images from Pd-rx 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 72789-106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pd-rx 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

72789105 Label (72789105)

72789105 Label (72789105)
Label for Metformin Hydrochloride Extended-release Tablets, USP 500 mg by PD-Rx Pharmaceuticals, Inc. The label states each extended-release tablet contains 500 mg metformin hydrochloride. It is an oral prescription drug packaged in a container of 90 tablets. Storage instructions and manufacturer details in Bangladesh are included. The NDC is 72789-105-90.*
FDA Label Image

72789106 Label (72789106)

72789106 Label (72789106)
Label for Metformin Hydrochloride Extended-release Tablets, USP 750 mg, marketed by PD-Rx Pharmaceuticals, Inc., available as Rx only. The label states 90 tablets per container and provides storage instructions. Manufactured by Beximco Pharmaceuticals LTD, Bangladesh. Includes barcode, NDC 72789-106-90, expiration date 10/2021, and lot number J19C06.*
FDA Label Image

Structural Formula (Image)

Structural Formula (Image)
Chemical structure of Metformin hydrochloride, a generic ingredient in Metformin hydrochloride ER tablets. The diagram shows the molecular arrangement including functional groups and the associated hydrochloride (HCl).*

* 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.