Structure (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 01)
Moxifloxacin Hydrochloride Solution/ Drops
Product Images NDC 67296-2232
View Photos of 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 Moxifloxacin Hydrochloride (NDC 67296-2232). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Redpharm Drug, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 02)
This text provides details about an ophthalmic solution containing moxifloxacin hydrochloride. Each mL contains 5.45 mg, which is equivalent to moxifloxacin 5 mg. The solution is stored at 2°C to 25°C (36°F to 77°F) 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 NDC number is 70069-081-01, and the solution is for prescription use only.*
Image (1a4f432a C2b2 46bc 88fc 7379c2bbd0a2 03)
This is a description of Moxifloxacin Ophthalmic Solution, USP manufactured by Somerset Therapeutics, LLC in Somerset, NJ. It is a sterile solution for topical ophthalmic use only. Each mL contains 5.45 mg of moxifloxacin hydrochloride, which is equivalent to 5mg of moxifloxacin. The inactive ingredients include boric acid, sodium chloride, and water for injection. The usual dosage is one drop in the affected eye three times a day for 7 days. It should be stored at 2°C to 25°C. Each box contains 3mL of the solution.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
