NDC 54868-4528 Patanol
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4528 - Patanol
Product Packages
NDC Code 54868-4528-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 5 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4528?
What are the uses for Patanol?
Which are Patanol UNII Codes?
The UNII codes for the active ingredients in this product are:
- OLOPATADINE HYDROCHLORIDE (UNII: 2XG66W44KF)
- OLOPATADINE (UNII: D27V6190PM) (Active Moiety)
Which are Patanol 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 PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Patanol?
- RxCUI: 1111339 - olopatadine HCl 0.1 % Ophthalmic Solution
- RxCUI: 1111339 - olopatadine 1 MG/ML Ophthalmic Solution
- RxCUI: 1111339 - olopatadine 0.1 % Ophthalmic Solution
- RxCUI: 1111339 - olopatadine 1 MG/ML (as olopatadine HCl 1.11 MG/ML) Ophthalmic Solution
- RxCUI: 1111341 - Patanol 0.1 % 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".