Metoprolol Succinate Tablet, Film Coated, Extended Release
Product Images NDC 71205-800

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71205-800). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-800-30 (Image 12)

71205-800-30 (Image 12)
Label for Metoprolol Succinate 50 mg extended-release film-coated tablets, packaged in a quantity of 30. The label states each tablet contains 47.5 mg metoprolol succinate USP, equivalent to 50 mg metoprolol tartrate USP. Manufactured by Teva Pharmaceuticals USA, Inc., with packaging by Proficient Rx LP, Thousand Oaks, CA. The label includes barcode, NDC 71205-800-30, and storage information at 25°C (77°F).*
FDA Label Image

71205-801-30 (Image 13)

71205-801-30 (Image 13)
Packaging label for metoprolol succinate 100 mg extended-release (ER) tablets. The label shows a bottle containing 30 film-coated tablets, each capsule-shaped and debossed with a logo and '677' on one side. It is labeled as RX only and packaged by Proficient Rx LP. Manufacturer is Teva Pharmaceuticals USA, Inc. with storage at 25°C.*
FDA Label Image

1 (Image 2)

1 (Image 2)
The image shows the packaging label for metoprolol succinate 100 mg extended-release film-coated tablets. The label indicates it is an oral dosage form and includes information about the labeler, Proficient Rx LP. The cover design features a curved blue graphic element in the top left corner.*
FDA Label Image

1 (Image 3)

1 (Image 3)
The image shows a carton of metoprolol succinate extended-release film-coated tablets by Proficient Rx LP. It displays the product name with available strengths of 50 mg and 100 mg per tablet, indicating oral administration. The label includes dosage form and manufacturer details.*
FDA Label Image

2 (Image 5)

2 (Image 5)
Chemical structure of metoprolol succinate showing the molecular components including a substituted phenyl ring with associated functional groups and the succinate moiety.*
FDA Label Image

1 (Image 6)

1 (Image 6)
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, and total mortality hospitalization for heart failure, comparing metoprolol succinate extended-release versus placebo across various subgroups such as geography, NYHA class, ejection fraction, etiology, sex, race, and medical history.*
FDA Label Image

1 (Image 8)

1 (Image 8)
Label for metoprolol succinate 100 mg extended release film-coated tablets in oral tablet form, labeled by Proficient Rx LP. The packaging includes identifying information with the product name and strength clearly displayed.*
FDA Label Image

1 (Image 9)

1 (Image 9)
metoprolol succinate 50 mg extended-release film-coated tablets packaging label. The white carton displays the brand and generic name, strength as 50 mg, dosage form as extended-release tablets, and labeler Proficient Rx LP. The package appears to include 30 tablets for oral use.*

* 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.