Toprol
Product Images NDC 70347-200

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Toprol (NDC 70347-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aralez Pharmaceuticals Us 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

Image01

Label for TOPROL XL 25 mg extended-release tablets containing metoprolol succinate. The label indicates a package size of 100 tablets, is marked Rx only, and includes a caution to verify the product dispensed. It is manufactured for Aralez Pharmaceuticals US Inc. in Parsippany, NJ.*

FDA Label Image

Image02

TOPROL XL 25 mg extended-release tablets bulk package label from Aralez Pharmaceuticals US Inc. The label includes the active ingredient metoprolol succinate, caution to verify the product dispensed, and notes that the package contains 1000 tablets and is not intended for dispensing. The label also features storage instructions and a barcode.*

FDA Label Image

Image03

TOPROL XL 50 mg extended-release tablets containing metoprolol succinate are shown in a packaging label by Aralez Pharmaceuticals US Inc. The label includes dosage strength, count of 100 tablets, a caution box to verify the product dispensed, and regulatory information such as NDC 70347-050-02 and Rx only designation.*

FDA Label Image

Image04

TOPROL XL 50 mg extended-release tablets packaging label showing 1000 tablets bulk package. Contains metoprolol succinate as active ingredient. Label includes caution to verify product dispensed and states Rx only. Labeler is Aralez Pharmaceuticals US Inc. Includes NDC 70347-050-03 and storage instructions.*

FDA Label Image

Image05

TOPROL XL 100 mg extended-release tablets containing metoprolol succinate, with 100 tablets per bottle. The label includes a caution to verify the product dispensed and is produced by Aralez Pharmaceuticals US Inc. Additional labeling details include the NDC number 70347-100-02 and manufacturing information.*

FDA Label Image

Image06

TOPROL XL (metoprolol succinate) extended-release tablets 100 mg bulk package label from Aralez Pharmaceuticals US Inc. The label includes caution to verify the product dispensed, indicates Rx only, and states it is a bulk package not intended for dispensing. The NDC number and active ingredient details are also visible.*

FDA Label Image

Image07

TOPROL XL 200 mg extended-release tablets packaging label from Aralez Pharmaceuticals US Inc. The label indicates the active ingredient as metoprolol succinate and features a caution box stating 'Verify Product Dispensed.' The package contains 100 tablets and includes prescribing and manufacturing information, along with a barcode.*

FDA Label Image

Image08

Packaging label for TOPROL XL 200 mg extended-release tablets containing metoprolol succinate. The label indicates a bulk package of 1000 tablets, with caution to verify the product dispensed. It is labeled as Rx only and manufactured by Aralez Pharmaceuticals US Inc.*

FDA Label Image

Image09

A forest plot chart titled "Results for Subgroups in MERIT-HF," showing relative risk and 95% confidence intervals for total mortality, total mortality or all-cause hospitalization (time to first event), and total mortality or hospitalization for heart failure (time to first event). Subgroups include geographic location, NYHA class, ejection fraction, etiology, sex, race, and health conditions. The plot compares favorability between metoprolol succinate extended release tablets and placebo across these subgroups.*

FDA Label Image

Image10

Chemical structure diagram showing the molecular formula of the active ingredient associated with TOPROL XL. The structure includes two identical organic moieties each containing hydroxyl (OH), methoxy (OCH3), and amine components, paired with a separate molecular fragment containing carboxyl groups (COOH).*

* 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.