Zioptan
Product Images NDC 17478-609
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Zioptan (NDC 17478-609). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Akorn, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
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ZIOPTAN® is a sterile ophthalmic solution for topical application in the eye. It is used for the treatment of high eye pressure associated with open-angle glaucoma or ocular hypertension. Each 0.3 mL single-use container contains 4.5 micrograms of the active ingredient tafluprost along with glycerol, sodium dihydrogen phosphate dihydrate, disodium edetate, polysorbate 80, and other inactive ingredients. It is refrigerated at 2° to 8°C (36° to 46°F) and should be discarded immediately after use. The solution is distributed by Akorn, Inc. and is manufactured for Oak Pharmaceuticals, Inc. and formulated in France. It is prescribed to be used once daily, in the evening, as one drop in the affected eye(s).*
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ZIOPTAN® is a prescription drug used for topical application in eyes. It contains tafluprost ophthalmic solution to be stored refrigerated at 2° to 8°C. It is available in single-use containers for immediate use and contains active ingredients like Glycerol, Sodium Dihydrogen Phosphate Dihydrate, and others. Distributed by Akorn Inc. and Manufactured for Oak Pharmaceuticals, Inc. However, no indication or medical advice regarding its usage is provided in the given text.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.