NDC 50383-232 Dorzolamide Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50383 - Akorn
- 50383-232 - Dorzolamide Hydrochloride
Product Packages
NDC Code 50383-232-10
Package Description: 1 BOTTLE in 1 CARTON / 10 mL in 1 BOTTLE
Price per Unit: $1.28838 per ML
Product Details
What is NDC 50383-232?
What are the uses for Dorzolamide Hydrochloride?
Which are Dorzolamide Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- DORZOLAMIDE HYDROCHLORIDE (UNII: QZO5366EW7)
- DORZOLAMIDE (UNII: 9JDX055TW1) (Active Moiety)
Which are Dorzolamide Hydrochloride Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)
- WATER (UNII: 059QF0KO0R)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- MANNITOL (UNII: 3OWL53L36A)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Dorzolamide Hydrochloride?
- RxCUI: 310015 - dorzolamide HCl 2 % Ophthalmic Solution
- RxCUI: 310015 - dorzolamide 20 MG/ML Ophthalmic Solution
- RxCUI: 310015 - dorzolamide 2 % Ophthalmic Solution
- RxCUI: 310015 - dorzolamide 20 MG/ML (as dorzolamide HCl 22.3 MG/ML) Ophthalmic Solution
* Please review the disclaimer below.
Patient Education
Dorzolamide Ophthalmic
Ophthalmic dorzolamide is used to treat glaucoma, a condition in which increased pressure in the eye can lead to gradual loss of vision. Dorzolamide is in a class of medications called carbonic anhydrase inhibitors. It works by decreasing the pressure in the eye.
[Learn More]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".