Aggrenox
Product Images NDC 54868-5143

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 Aggrenox (NDC 54868-5143). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Physicians Total Care, 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

Aggrenox (60 capsules)

Aggrenox (60 capsules)
Label for Aggrenox 25/200 mg, distributed by Physicians Total Care, Inc. The label shows the NDC number 54868-5143, a lot number, expiration date 01/60, and indicates manufacturing by Boehringer Ingelheim Pharma in Germany. A barcode is also visible at the bottom.*
FDA Label Image

Structural Formula Of Dipyridamole. (Aggrenox Struct1)

Structural Formula Of Dipyridamole. (Aggrenox Struct1)
Chemical structure of the active ingredient associated with Aggrenox, showing a complex molecule with multiple nitrogen atoms and hydroxyl groups, molecular formula C24H40N8O4, and molecular weight 504.63.*
FDA Label Image

Structural Formula Of Benzoic Acid. (Aggrenox Struct2)

Structural Formula Of Benzoic Acid. (Aggrenox Struct2)
Chemical structure diagram depicting acetylsalicylic acid (aspirin), with molecular formula C9H8O4 and molecular weight 180.16, commonly related to Aggrenox components.*
FDA Label Image

Figure 1. (Aggrenox Figure1)

Figure 1. (Aggrenox Figure1)
A line chart depicting the cumulative stroke rate percentage over 24 months of follow-up among different treatment groups, including Aggrenox, aspirin (ASA), extended-release dipyridamole (ER-DP), and placebo. The chart shows comparative stroke rates for these groups across time.*

* 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.