Metoprolol Tartrate
Product Images NDC 10544-124

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 10544-124). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Blenheim Pharmacal, 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

Label Graphic-metoprolol 100mg 90s (Label Graphic Metoprolol 100mg 90s)

Label for Metoprolol Tartrate Tablets, USP 100mg, containing 90 tablets. The label states Rx only, with storage instructions to keep at controlled room temperature 15°-30°C (59°-86°F) in a light-resistant container and out of reach of children. The label includes the NDC number 10544-553-90 and manufacturer information for Blenheim Pharmacal, Inc. It also features a barcode and batch details with placeholder lot and expiration dates.*

FDA Label Image

Chemical-structure (Image 01)

Chemical structure of Metoprolol Tartrate, showing the metoprolol molecule paired with tartrate as a salt form. The image displays two connected chemical structures representing the active drug ingredient and its tartrate component.*

FDA Label Image

Label Graphic-metoprolol 50mg 30s (Metoprolol Fig1)

Metoprolol Tartrate Tablets USP 50 mg label for a 30-tablet package by Blenheim Pharmacal, Inc. The label includes NDC 10544-124-30 and MFG 57664-166-58. It states prescription only, storage instructions at 15°-30°C, and a warning to keep out of reach of children. The label also includes batch and expiration date placeholders and barcode information.*

* 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.