Metoprolol Tartrate Tablet
Product Images NDC 52817-250

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Metoprolol Tartrate (NDC 52817-250). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma Llc, 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

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-10)

Label for Metoprolol Tartrate Tablets, USP 100 mg oral tablets by TruPharma LLC. The label states 100 tablets per container, with NDC 52817-254-10. It includes storage instructions, distributor and manufacturer details (Rubicon Research Ltd., India), and child-resistant container warnings.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 100 mg (NDC 52817-254-00)

Label for Metoprolol Tartrate Tablets USP 100 mg oral tablets by TruPharma LLC. The label states the product contains 100 mg metoprolol tartrate per uncoated tablet and comes in a bottle of 1,000 tablets. It includes storage instructions, manufacturer information (Rubicon Research Ltd., India), and barcode.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-10)

Label for Metoprolol Tartrate Tablets USP 25 mg, oral tablets supplied in a package of 100 tablets. The label includes dosage strength (25 mg), distributor TruPharma LLC (Tampa, FL), and manufacturer Rubicon Research Ltd. (India). It features storage instructions, child safety warnings, and barcodes on both sides of the label.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 25 mg (NDC 52817-250-00)

Metoprolol Tartrate Tablets USP 25 mg label showing a blue box with product name and strength, indicating 1,000 tablets, Rx only. Distributed by TruPharma LLC and manufactured by Rubicon Research Ltd. Storage instructions and warnings to keep medication out of reach of children are present. A barcode and TruPharma logo are visible, along with an overprinting area section.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 37.5 mg (NDC 52817-251-10)

Label for Metoprolol Tartrate Tablets USP 37.5 mg, oral tablets, packaged in a container of 100 tablets. The label includes storage instructions to keep between 20°C to 25°C and out of reach of children. Distributed by TruPharma LLC and manufactured by Rubicon Research Ltd. in India. The NDC number includes 52817-251-10.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-10)

Label for Metoprolol Tartrate Tablets USP, 50 mg, oral tablet dosage form. The label states the product contains 50 mg Metoprolol Tartrate per uncoated tablet with a 100-tablet count. Distributed by TruPharma LLC, manufactured by Rubicon Research Ltd. in India. Storage instructions and caution about child safety are included. Contains barcodes and a marked overprinting area.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 50 mg (NDC 52817-252-00)

Label for Metoprolol Tartrate Tablets, USP 50 mg by TruPharma LLC, distributed in Tampa, FL, and manufactured by Rubicon Research Ltd. The label shows a package of 1,000 uncoated tablets with storage instructions and safety warnings, including keeping medication out of reach of children and storing at 20°C to 25°C.*

FDA Label Image

Metoprolol Tartrate Tablets, Usp 75 mg (NDC 52817-253-10)

Label for Metoprolol Tartrate Tablets USP 75 mg, oral tablets supplied in a bottle of 100 count. The label displays the active ingredient strength, usage instructions to see package insert, storage conditions, and child-resistant packaging instructions. Distributed by TruPharma LLC, manufactured by Rubicon Research Ltd., India. Includes NDC 52817-253-10 and a barcode.*

FDA Label Image

Metoprolol Tartrate Tablet Structure (Metoprolol Tartrate Tabs Structure)

Chemical structure diagram showing the molecular formula of Metoprolol Tartrate, a beta-blocker active ingredient used in oral tablet form.*

* 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.