NDC 68071-4650 Latanoprost
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What is NDC 68071-4650?
What are the uses for Latanoprost?
Which are Latanoprost UNII Codes?
The UNII codes for the active ingredients in this product are:
- LATANOPROST (UNII: 6Z5B6HVF6O)
- LATANOPROST (UNII: 6Z5B6HVF6O) (Active Moiety)
Which are Latanoprost 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)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM (UNII: 3980JIH2SW)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
What is the NDC to RxNorm Crosswalk for Latanoprost?
- RxCUI: 314072 - latanoprost 0.005 % Ophthalmic Solution
- RxCUI: 314072 - latanoprost 0.05 MG/ML Ophthalmic Solution
- RxCUI: 314072 - latanoprost 125 MCG per 2.5 ML Ophthalmic Solution
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Patient Education
Latanoprost Ophthalmic
Latanoprost ophthalmic is used to treat glaucoma (a condition in which increased pressure in the eye can lead to gradual loss of vision) and ocular hypertension (a condition which causes increased pressure in the eye). Latanoprost is in a class of medications called prostaglandin analogs. It lowers pressure in the eye by increasing the flow of natural eye fluids out of 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".