NDC 54868-4972 Foradil
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4972 - Foradil
Product Characteristics
Product Packages
NDC Code 54868-4972-1
Package Description: 10 BLISTER PACK in 1 BOX / 6 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 54868-4972?
What are the uses for Foradil?
Which are Foradil UNII Codes?
The UNII codes for the active ingredients in this product are:
- FORMOTEROL FUMARATE (UNII: P3T5QA5J9N)
- FORMOTEROL (UNII: 5ZZ84GCW8B) (Active Moiety)
Which are Foradil 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 Foradil?
- RxCUI: 1246326 - formoterol fumarate 12 MCG Inhalation Powder
- RxCUI: 1246326 - formoterol fumarate 0.012 MG Inhalation Powder
- RxCUI: 1246328 - Foradil 12 MCG Inhalation Powder
- RxCUI: 1246328 - formoterol fumarate 0.012 MG Inhalation Powder [Foradil]
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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".