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Moxifloxacin Hydrochloride Solution/ Drops
Product Images NDC 70069-081
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Moxifloxacin Hydrochloride (NDC 70069-081). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Somerset Therapeutics, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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This is a description for an ophthalmic solution containing moxifloxacin hydrochloride. Each milliliter of the solution contains 5.45 mg of moxifloxacin hydrochloride, equivalent to 5 mg of moxifloxacin. The solution is stored at a temperature range of 2°C to 25°C and is intended for topical ophthalmic use only. It comes in a 3mL bottle with a tamper-evident seal and is manufactured for Somerset Therapeutics, LLC in Somerset, NJ. The product is sterile and made in India. The text includes NDC and RX only labels, along with specific storage instructions.*
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This is a detailed label of Moxifloxacin Ophthalmic Solution, USP, manufactured for Somerset Therapeutics in New Jersey. It is made in India and contains moxifloxacin hydrochloride for topical ophthalmic use. Each mL contains 5.45 mg of moxifloxacin hydrochloride. The solution is sterile and should be stored between 2°C to 25°C. The usual dosage is one drop in the affected eye three times a day for 7 days. The solution comes in a 3mL bottle with a tamper-evident seal and is for prescription use only. Contact number for customer care is provided.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
