NDC 54868-4793 Restasis
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4793 - Restasis
Product Packages
NDC Code 54868-4793-1
Package Description: 30 VIAL, SINGLE-DOSE in 1 TRAY / .4 mL in 1 VIAL, SINGLE-DOSE
Product Details
What is NDC 54868-4793?
What are the uses for Restasis?
Which are Restasis UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYCLOSPORINE (UNII: 83HN0GTJ6D)
- CYCLOSPORINE (UNII: 83HN0GTJ6D) (Active Moiety)
Which are Restasis 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- CASTOR OIL (UNII: D5340Y2I9G)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Restasis?
- RxCUI: 2572292 - cycloSPORINE 0.05 % in 0.4 ML Ophthalmic Emulsion
- RxCUI: 2572292 - 0.4 ML cyclosporine 0.5 MG/ML Ophthalmic Suspension
- RxCUI: 2572292 - cyclosporine 0.05 % per 0.4 ML Ophthalmic Emulsion
- RxCUI: 2572292 - cyclosporine 0.5 MG/ML per 0.4 ML Ophthalmic Emulsion
- RxCUI: 2572293 - Restasis 0.05 % in 0.4 ML Ophthalmic Emulsion
* Please review the disclaimer below.
[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".