NDC 54868-5968 Travatan Z
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5968 - Travatan Z
Product Packages
NDC Code 54868-5968-0
Package Description: 1 BOTTLE in 1 CARTON / 5 mL in 1 BOTTLE
NDC Code 54868-5968-1
Package Description: 1 BOTTLE in 1 CARTON / 2.5 mL in 1 BOTTLE
Product Details
What is NDC 54868-5968?
What are the uses for Travatan Z?
Which are Travatan Z UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRAVOPROST (UNII: WJ68R08KX9)
- TRAVOPROST (UNII: WJ68R08KX9) (Active Moiety)
Which are Travatan Z 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:
- POLYOXYL 40 CASTOR OIL (UNII: 4ERD2076EF)
- BORIC ACID (UNII: R57ZHV85D4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Travatan Z?
- RxCUI: 284008 - travoprost 0.004 % Ophthalmic Solution
- RxCUI: 284008 - travoprost 0.04 MG/ML Ophthalmic Solution
- RxCUI: 284008 - travoprost 40 MCG/ML Ophthalmic Solution
- RxCUI: 285032 - TRAVATAN Z 0.004 % Ophthalmic Solution
- RxCUI: 285032 - travoprost 0.04 MG/ML Ophthalmic Solution [Travatan]
* 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".