Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 59651-758

View Photos of 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 Metoprolol Tartrate (NDC 59651-758). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (37.5 mg (100 Tablet Bottle))

Package Label-principal Display Panel (37.5 mg (100 Tablet Bottle))
Label for Metoprolol Tartrate Tablets, USP 37.5 mg, film-coated oral tablets by Aurobindo Pharma Limited. The label states a package size of 100 tablets and includes storage instructions, distributor information, and a barcode. The label design features the Aurobindo logo and highlights the active ingredient strength prominently in purple.*
FDA Label Image

Package Label-principal Display Panel (75 mg (100 Tablet Bottle))

Package Label-principal Display Panel (75 mg (100 Tablet Bottle))
Label for Metoprolol Tartrate Tablets, USP 75 mg film-coated tablets. The package contains 100 tablets and is distributed by Aurobindo Pharma USA, Inc. The label includes storage instructions, dosage note to see package insert, and an NDC number 59651-760-01. It specifies the drug is made in India by Aurobindo Pharma Limited.*
FDA Label Image

Chemical Structure (Metoprolol Str)

Chemical Structure (Metoprolol Str)
Chemical structure of Metoprolol Tartrate, showing the molecular components including aromatic ring, ether linkages, hydroxyl groups, and tartrate salt structure.*

* 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.