Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 43063-821

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 43063-821). 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

43063821 Label (43063821)

Label for Metoprolol Tartrate USP 50 mg film-coated tablets, containing 30 tablets per bottle. The label displays dosage strength, quantity, and manufacturer PD-Rx Pharmaceuticals, Inc. It includes safety warnings, lot number D22E34, and expiration date 04/2024. The NDC is 43063-821-30, with additional barcode and regulatory information.*

FDA Label Image

Metoprolol-structure (Metoprolol Str)

Chemical structure diagram of Metoprolol Tartrate showing its molecular arrangement, including the tartrate portion represented separately with hydrogen bonds indicated.*

* 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.