NDC 54868-4277 Alrex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4277 - Alrex
Product Packages
NDC Code 54868-4277-0
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER
NDC Code 54868-4277-1
Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 5 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 54868-4277?
What are the uses for Alrex?
Which are Alrex UNII Codes?
The UNII codes for the active ingredients in this product are:
- LOTEPREDNOL ETABONATE (UNII: YEH1EZ96K6)
- LOTEPREDNOL (UNII: Z8CBU6KR16) (Active Moiety)
Which are Alrex 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)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- POVIDONE (UNII: FZ989GH94E)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TYLOXAPOL (UNII: Y27PUL9H56)
What is the NDC to RxNorm Crosswalk for Alrex?
- RxCUI: 213262 - Alrex 0.2 % Ophthalmic Suspension
- RxCUI: 213262 - loteprednol etabonate 2 MG/ML Ophthalmic Suspension [Alrex]
- RxCUI: 213262 - Alrex 2 MG/ML Ophthalmic Suspension
- RxCUI: 311381 - loteprednol etabonate 0.2 % Ophthalmic Suspension
- RxCUI: 311381 - loteprednol etabonate 2 MG/ML Ophthalmic Suspension
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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".