NDC 17478-604 Cosopt Pf
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What is NDC 17478-604?
What are the uses for Cosopt Pf?
Which are Cosopt Pf 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 ANHYDROUS (UNII: 5JKY92S7BR) (Active Moiety)
Which are Cosopt Pf 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)
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Cosopt Pf?
- RxCUI: 1922783 - dorzolamide 2 % / timolol 0.5 % PF Ophthalmic Solution
- RxCUI: 1922783 - Preservative-Free dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution
- RxCUI: 1922784 - COSOPT PF 2 % / 0.5 % Ophthalmic Solution
- RxCUI: 1922784 - Preservative-Free dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution [Cosopt]
- RxCUI: 1922784 - Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution
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Patient Education
Dorzolamide and Timolol Ophthalmic
The combination of dorzolamide and timolol is used to treat eye conditions, including glaucoma and ocular hypertension, in which increased pressure can lead to a gradual loss of vision. Dorzolamide and timolol is used for patients whose eye condition has not responded to another medication. Dorzolamide is in a class of medications called topical carbonic anhydrase inhibitors. Timolol is in a class of medications called topical beta blockers. Dorzolamide and timolol lowers pressure in the eye by decreasing the production of natural fluids in the eye.
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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".