Clopidogrel
Product Images NDC 76519-1016

3 FDA label images from H.j. Harkins Company Inc · 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 Clopidogrel (NDC 76519-1016). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by H.j. Harkins Company 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

76519 1016.jpg (76519 1016)

76519 1016.jpg (76519 1016)
Label for Clopidogrel 75mg tablets, repackaged by H.J. Harkins Company Inc in Grover Beach, California. The label features multiple drug identification sections listing NDC 76519-1016-XX, expiration date 06/30/19, lot number BCA8717A, and placeholder quantity XX. Manufacturer is Macleods 3334 with lot #BCA8717A. Includes caution statement about federal law and prescription use.*
FDA Label Image

Figure 1.jpg (Figure 1)

Figure 1.jpg (Figure 1)
A horizontal bar plot illustrating the effect of different co-administered proton pump inhibitors (PPIs) on the active metabolite area under the curve (AUC) of Clopidogrel. It shows mean values with 90% confidence intervals for Dexlansoprazole 60 mg, Lansoprazole 30 mg, Pantoprazole 80 mg, and Omeprazole 80 mg, comparing changes relative to Clopidogrel administered alone.*
FDA Label Image

Clopidogrel.jpg (Clopidogrel)

Clopidogrel.jpg (Clopidogrel)
Chemical structure of Clopidogrel hydrogen sulfate showing a bicyclic thienopyridine ring system connected to a methyl ester and chlorophenyl group with a sulfate moiety.*

* 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.