Metformin Hydrochloride Tablet, Extended Release
Product Images NDC 72789-455

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metformin Hydrochloride (NDC 72789-455). 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.

FDA Label Image

Formula (5b0e9cbd A325 401b 9c72 38a96d3afd66 01)

Chemical structure of metformin hydrochloride, showing its molecular arrangement with distinct methyl groups (CH3), nitrogen atoms, and hydrochloride component, consistent with the active ingredient in METFORMIN HYDROCHLORIDE extended-release tablets.*

FDA Label Image

Image (5b0e9cbd A325 401b 9c72 38a96d3afd66 104 2)

METFORMIN HYDROCHLORIDE 500 mg extended release oral tablets blister pack. The label shows individual tablets in a 10-count blister with each tablet embossed. The packaging displays the product name, strength, dosage form, and the labeler PD-Rx Pharmaceuticals, Inc.*

FDA Label Image

Image (5b0e9cbd A325 401b 9c72 38a96d3afd66 26 1)

METFORMIN HYDROCHLORIDE 500 mg extended release oral tablet label. The label displays drug name, strength, dosage form, route, and manufacturer PD-Rx Pharmaceuticals, Inc. It includes standard drug labeling text elements and design in black and white.*

FDA Label Image

72789455 Label (72789455)

Label for Metformin Hydrochloride Extended Release (HCL ER) 500 mg tablets by PD-Rx Pharmaceuticals, Inc. The bottle contains 30 tablets. The label includes the NDC 72789-455-30, dosage strength, lot number L24A84, and expiration date 01/2026. Warnings include 'Do not crush or chew' and 'Keep out of reach of children.'*

* 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.