Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 82804-165

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 82804-165). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

82804-165-90 (Image 01)

82804-165-90 (Image 01)
Label for Metoprolol Tartrate 50 mg film-coated tablets by Proficient Rx LP. The package contains 90 tablets. Tablets are described as pink, round, biconvex, debossed with 'R 50' on one side and scored on the other. The label includes storage instructions and manufacturer information from Rubicon Research Private Limited, India. Multiple barcodes and QR codes are visible along with NDC 82804-165-90.*
FDA Label Image

Metoprolol Tartrate Tabs Usp 50mg Image

Metoprolol Tartrate Tabs Usp 50mg Image
Metoprolol Tartrate 50 mg film-coated tablet showing round, pink tablet with imprint "R 50" on one side. The image depicts the tablet's color, shape, and imprint used for identification. This oral dosage form is part of the product line by Proficient Rx LP.*
FDA Label Image

Metoprolol Tartrate Tablets, Usp Chemical Structure (Metoprolol Tartrate Tabs Usp Structure)

Metoprolol Tartrate Tablets, Usp Chemical Structure (Metoprolol Tartrate Tabs Usp Structure)
Chemical structure diagram showing the molecular structure of Metoprolol Tartrate, the active ingredient in the product Metoprolol Tartrate 50 mg film-coated tablets by Proficient Rx LP.*

* 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.