NDC 54868-5547 Asmanex
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54868-5547?
What are the uses for Asmanex?
Which are Asmanex UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOMETASONE FUROATE (UNII: 04201GDN4R)
- MOMETASONE (UNII: 8HR4QJ6DW8) (Active Moiety)
Which are Asmanex 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
What is the NDC to RxNorm Crosswalk for Asmanex?
- RxCUI: 746810 - mometasone furoate 220 MCG/INHAL Dry Powder Inhaler, 14 ACTUAT
- RxCUI: 746810 - 14 ACTUAT mometasone furoate 0.22 MG/ACTUAT Dry Powder Inhaler
- RxCUI: 746810 - mometasone furoate 220 MCG/ACTUAT Dry Powder Inhaler, 14 ACTUAT
- RxCUI: 746811 - Asmanex Twisthaler 220 MCG/INHAL Dry Powder Inhaler, 14 ACTUAT
- RxCUI: 746811 - 14 ACTUAT mometasone furoate 0.22 MG/ACTUAT Dry Powder Inhaler [Asmanex]
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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".