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Moxifloxacin Solution/ Drops
Product Images NDC 68180-422
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This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin (NDC 68180-422). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lupin Pharmaceuticals, 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.
Product Images & Figures Index
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This is a description of a prescription drug with the NDC code 68180-422-01. The drug contains Moxifloxacin hydrochloride USP 5.45 mg per mL of solution, ophthalmic equivalent to moxifloxacin 5 mg g. It is manufactured by an entity called Lupin and is intended for use in the eyes only. The solution is sterile and the product comes in a 3mL package with an expiration date of 28/6/2010.*
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This is a product description for Moxifloxacin Ophthalmic Solution, USP, used for eye treatment. One mL of the solution contains 5.45 mg of moxifloxacin hydrochloride USP, which is equivalent to 5mg of Moxifloxacin. The solution also has inactive ingredients such as borle acld, sodlum chlorids, and water for injection that may contain hydrochlorlc acld and/or sodium hydroxide to alter pH. The product, manufactured by Lupin Limited, is for use in eyes only and is sterile. The recommended dosage is one drop in the affected eye three times a day for seven days, as prescribed. The product should be stored at 2°C to 25°C (36°FW77°F), and needs to be kept out of reach of children.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
