Metoprolol Succinate Tablet, Extended Release
Product Images NDC 71335-9749

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Metoprolol Succinate (NDC 71335-9749). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Image (00df8655 C4ff 481f Bd4f E43b69b3a059 01)

Image (00df8655 C4ff 481f Bd4f E43b69b3a059 01)
Chemical structure diagram of metoprolol succinate, showing the molecular arrangement of metoprolol linked to succinate components.*
FDA Label Image

Merit Hf (00df8655 C4ff 481f Bd4f E43b69b3a059 02)

Merit Hf (00df8655 C4ff 481f Bd4f E43b69b3a059 02)
A forest plot titled 'Results for Subgroups in MERIT-HF' showing relative risk and 95% confidence intervals for metoprolol succinate extended-release tablets versus placebo across various clinical subgroups. The chart displays comparisons for outcomes including total mortality, total mortality or all-cause hospitalization, and total mortality or hospitalization for heart failure, with subgroup categories listed on the left and risk favored either metoprolol succinate or placebo on the horizontal axis.*
FDA Label Image

Label (Lbl713359749)

Label (Lbl713359749)
METOPROLOL SUCCINATE 50 mg extended-release tablets label showing the NDC 71335-9749-1. The label includes dosage strength 50 mg, package quantity 30 tablets, and indicates Rx only. It also states the product is repackaged by Bryant Ranch Prepack, Inc. and manufactured by Cipla Ltd. Storage and safety instructions are included.*

* 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.