Metoprolol Tartrate Tablet
Product Images NDC 46708-292

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 46708-292). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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

30 Tablets In 1 Hdpe Bottle (Metoprolol 100mg)

30 Tablets In 1 Hdpe Bottle (Metoprolol 100mg)
This appears to be a prescription drug label for a medication called Netoprolol Tartrate, supplied by a company called Nembic Pharmaceuticals Limited. The dosage form is tablets, with a quantity of 30 tablets per bottle (NDC 46708-292-30). The label also includes a physical address for the company in India and a warning about keeping the container tightly closed (Kesp ontaine gl cosed).*
FDA Label Image

30 Tablets In 1 Hdpe Bottle (Metoprolol 25mg)

30 Tablets In 1 Hdpe Bottle (Metoprolol 25mg)
This is a label of a medication called Netoprolol Tartrate, with a controlled 1 tablet, USP. It is stored at a temperature between 20-25° C and should be kept away from children. The manufacturer is Y Nembic Pharmaceutcals Limited based in India.*
FDA Label Image

30 Tablets In 1 Hdpe Bottle (Metoprolol 50mg)

30 Tablets In 1 Hdpe Bottle (Metoprolol 50mg)
Product description: Gabemasze (Netoprolol Tartrate) tablets, USP. The product should be stored at 20° to 25°C and protected from moisture. The container should be kept tightly closed and out of reach of children. The manufacturer is Nembic Pharmaceuticals Limited with a license number of G859.*
FDA Label Image

Structure (Metoprolol Str)

* 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.