Metoprolol Tartrate
Product Images NDC 67296-0729

3 FDA label images from Redpharm Drug 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 Metoprolol Tartrate (NDC 67296-0729). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug 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

Metoprolol 25mg (Sdistributi19050715120 0001)

Metoprolol 25mg (Sdistributi19050715120 0001)
Label for Metoprolol tartrate 25 mg tablets, 30 count, NDC 67296-0729-1. Label indicates prescription only, manufactured by Sun Pharmaceutical Industries Ltd in India, and distributed by RedPharm Drug, Inc. in Eden Prairie, MN. It includes lot number KT0682X1 and expiration date 05/20, with storage instructions to keep at 20-25°C (68-77°F). Barcode and QR code present.*
FDA Label Image

Structure (Metoprolol 1)

Structure (Metoprolol 1)
Chemical structure diagram showing the molecular formula and composition of Metoprolol tartrate. The image depicts the structural arrangement of atoms and bonds in the compound including the metoprolol moiety and the tartrate counterion.*
FDA Label Image

Table (Metoprolol 2)

Table (Metoprolol 2)
A data table comparing the incidence percentages of various cardiac-related adverse events including hypotension, bradycardia, second- or third-degree heart block, first-degree heart block, and heart failure between Metoprolol and placebo groups.*

* 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.