Metoprolol Tartrate Tablet, Film Coated
Product Images NDC 51407-110

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 51407-110). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-109-10lb.jpg (51407 109 10lb)

Label for Metoprolol Tartrate 25 mg tablets, USP by Golden State Medical Supply, Inc. The label states the quantity as 1,000 tablets and includes a National Drug Code (NDC) 51407-109-10. It also contains dosing instructions to see the package insert and storage information at 20° to 25°C (68° to 77°F). The label indicates the product is Rx only and provides manufacturer details.*

FDA Label Image

51407-110-10lb.jpg (51407 110 10lb)

Metoprolol Tartrate 50 mg tablets label, USP, containing 1,000 film-coated oral tablets. The label includes the NDC 51407-110-10 and highlights that the product is prescription only (Rx only). The manufacturer is Golden State Medical Supply, Inc. Storage instructions indicate to keep at controlled room temperature (20 to 25°C).*

FDA Label Image

51407-111-01lb.jpg (51407 111 01lb)

Label for Metoprolol Tartrate tablets, USP 100 mg by Golden State Medical Supply, Inc. The label indicates a package of 100 film-coated tablets for oral use. It includes the NDC number 51407-111-01 and storage instructions at 20° to 25°C (68° to 77°F). The label states prescription use only and lists handling and safety information.*

FDA Label Image

Metoprolol Tartrate Structural Formula (Image 01)

Chemical structure of metoprolol tartrate, showing the molecular arrangement of the metoprolol moiety with its tartrate component. The diagram includes the aromatic ring, ether linkages, alcohol, amine groups, and the tartaric acid portion.*

* 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.