Human Drugs View

Product Information
Registration Number DRP-13772
Generic Name Dorzolamide (as hydrochloride)
Brand Name Lumedor
Dosage Strength 20 mg/mL (2% w/v)
Dosage Form Ophthalmic Solution (Eye Drops)
Classification Prescription Drug (RX)
Pharmacologic Category Antiglaucoma (Carbonic anhydrase inhibitor)
Packaging White Opaque LDPE Plastic vial with White colored Cap x 10 mL (Box of 1's)
Manufacturer Axa Parenterals Limited
Country of Origin India
Trader
Importer Brady Pharma Inc.
Distributor Brady Pharma Inc.
Application Type Initial (Reconstruction)
Issuance Date 12 August 2024
Expiry Date 17 April 2028