NDC 17478-173 Xopenex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17478 - Akorn
- 17478-173 - Xopenex
Product Packages
NDC Code 17478-173-24
Package Description: 2 POUCH in 1 CARTON / 12 VIAL, SINGLE-DOSE in 1 POUCH (17478-173-12) / 3 mL in 1 VIAL, SINGLE-DOSE
Price per Unit: $2.53087 per ML
Product Details
What is NDC 17478-173?
What are the uses for Xopenex?
Which are Xopenex UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVALBUTEROL HYDROCHLORIDE (UNII: WDQ1526QJM)
- LEVALBUTEROL (UNII: EDN2NBH5SS) (Active Moiety)
Which are Xopenex 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SULFURIC ACID (UNII: O40UQP6WCF)
- WATER (UNII: 059QF0KO0R)
- NITROGEN (UNII: N762921K75)
What is the NDC to RxNorm Crosswalk for Xopenex?
- RxCUI: 242754 - levalbuterol HCl 1.25 MG in 3 ML Inhalation Solution
- RxCUI: 242754 - levalbuterol 0.417 MG/ML Inhalation Solution
- RxCUI: 242754 - levalbuterol 1.25 MG (as levalbuterol HCl 1.44 MG) per 3 ML Inhalation Solution
- RxCUI: 261136 - Xopenex 0.63 MG in 3 ML Inhalation Solution
- RxCUI: 261136 - levalbuterol 0.21 MG/ML Inhalation Solution [Xopenex]
* Please review the disclaimer below.
Patient Education
Levalbuterol Oral Inhalation
Levalbuterol is used to prevent or relieve the wheezing, shortness of breath, coughing, and chest tightness caused by lung disease such as asthma and chronic obstructive pulmonary disease (COPD; a group of diseases that affect the lungs and airways). Levalbuterol is in a class of medications called beta agonists. It works by relaxing and opening air passages to the lungs to make breathing easier.
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* 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".