Dorzolamide Hydrochloride Solution
Product Images NDC 69315-304
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Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Dorzolamide Hydrochloride (NDC 69315-304). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Leading Pharma, 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.
Product Images & Figures Index
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Carton (Edaa4f35 98f2 4429 8730 Babeb871b05b 08)
This is a description of Dorzolamide HCI Ophthalmic Solution USP 2%. It is a sterile solution that should be stored at 20°C-25°C and protected from light. The solution contains 22.3mg Dorzolamide Hydrochloride and various inactive ingredients. The product should be dispensed from the original unopened container to avoid contamination. The usual dosage is to be determined from the prescribing information. The product should be retained in the carton until the contents are used. To use the product, remove the dust cover, unscrew the cap, dispense the drops, and then replace the cap with gentle pressure. The product is distributed by Leading Pharma, LLC.*
Carton 10 mL (Edaa4f35 98f2 4429 8730 Babeb871b05b 09)
This product is a sterile ophthalmic solution used for topical application on the eye. It contains dorzolamide hydrochloride, hydroxyethyl cellulose, mannitol, sodium citrate dihydrate, sodium hydroxide, and water for injection. It also has benzalkonium chloride as a preservative. The instructions for use are printed on the label with the recommendation that contents be kept in its original box until used. It is manufactured in India by FDC Limited, and distributed by Leading Pharma, LLC in Fairfield, NJ.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.