NDC 33261-874 Advair Diskus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-874 - Advair
Product Packages
NDC Code 33261-874-01
Package Description: 60 POWDER in 1 INHALER
Product Details
What is NDC 33261-874?
What are the uses for Advair Diskus?
Which are Advair Diskus UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALMETEROL XINAFOATE (UNII: 6EW8Q962A5)
- SALMETEROL (UNII: 2I4BC502BT) (Active Moiety)
- FLUTICASONE PROPIONATE (UNII: O2GMZ0LF5W)
- FLUTICASONE (UNII: CUT2W21N7U) (Active Moiety)
Which are Advair Diskus 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:
- LACTOSE (UNII: J2B2A4N98G)
What is the NDC to RxNorm Crosswalk for Advair Diskus?
- RxCUI: 896184 - fluticasone propionate/salmeterol 100/50 MCG/INHAL Dry Powder Inhaler, 60 Blisters
- RxCUI: 896184 - 60 ACTUAT fluticasone propionate 0.1 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler
- RxCUI: 896184 - fluticasone propionate 0.1 MG/ACTUAT / salmeterol 0.05 MG/ACTUAT Dry Powder Inhaler, 60 ACTUAT
- RxCUI: 896184 - fluticasone propionate 100 MCG / salmeterol 50 MCG (salmeterol xinafoate 72.5 MCG) per ACTUAT Dry Powder Inhaler, 60 ACTUAT
- RxCUI: 896185 - ADVAIR DISKUS 100/50 MCG/INHAL Dry Powder Inhaler, 60 Blisters
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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".