NDC 54868-4279 Cosopt
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 54868-4279?
What are the uses for Cosopt?
Which are Cosopt UNII Codes?
The UNII codes for the active ingredients in this product are:
- DORZOLAMIDE HYDROCHLORIDE (UNII: QZO5366EW7)
- DORZOLAMIDE (UNII: 9JDX055TW1) (Active Moiety)
- TIMOLOL MALEATE (UNII: P8Y54F701R)
- TIMOLOL (UNII: 817W3C6175) (Active Moiety)
Which are Cosopt 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:
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- MANNITOL (UNII: 3OWL53L36A)
- TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cosopt?
- RxCUI: 1923432 - dorzolamide HCl 2 % / timolol maleate 0.5 % Ophthalmic Solution
- RxCUI: 1923432 - dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution
- RxCUI: 1923432 - dorzolamide 2 % / timolol 0.5 % Ophthalmic Solution
- RxCUI: 1923432 - dorzolamide 20 MG/ML (as dorzolamide HCl 22.26 MG/ML) / timolol 5 MG/ML (as timolol maleate 6.83 MG/ML) Ophthalmic Solution
- RxCUI: 1923433 - COSOPT 2 % / 0.5 % Ophthalmic Solution
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[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".