NDC 54868-4798 Vigamox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4798 - Vigamox
Product Packages
NDC Code 54868-4798-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 3 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4798?
What are the uses for Vigamox?
Which are Vigamox UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOXIFLOXACIN HYDROCHLORIDE (UNII: C53598599T)
- MOXIFLOXACIN (UNII: U188XYD42P) (Active Moiety)
Which are Vigamox 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:
- BORIC ACID (UNII: R57ZHV85D4)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- WATER (UNII: 059QF0KO0R)
- HYDROCHLORIC ACID (UNII: QTT17582CB)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
What is the NDC to RxNorm Crosswalk for Vigamox?
- RxCUI: 403818 - moxifloxacin HCl 0.5 % Ophthalmic Solution
- RxCUI: 403818 - moxifloxacin 5 MG/ML Ophthalmic Solution
- RxCUI: 403818 - moxifloxacin (as moxifloxacin HCl) 0.5 % Ophthalmic Solution
- RxCUI: 404473 - VIGAMOX 0.5 % Ophthalmic Solution
- RxCUI: 404473 - moxifloxacin 5 MG/ML Ophthalmic Solution [Vigamox]
* 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".