NDC 54868-5109 Spiriva
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Product Characteristics
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Product Details
What is NDC 54868-5109?
What are the uses for Spiriva?
Which are Spiriva UNII Codes?
The UNII codes for the active ingredients in this product are:
- TIOTROPIUM BROMIDE MONOHYDRATE (UNII: L64SXO195N)
- TIOTROPIUM (UNII: 0EB439235F) (Active Moiety)
Which are Spiriva 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 MONOHYDRATE (UNII: EWQ57Q8I5X)
What is the NDC to RxNorm Crosswalk for Spiriva?
- RxCUI: 485032 - tiotropium 18 MCG Inhalation Powder
- RxCUI: 485032 - tiotropium 0.018 MG Inhalation Powder
- RxCUI: 485032 - tiotropium 18 MCG (tiotropium bromide 22.5 MCG) Inhalation Powder
- RxCUI: 580261 - SPIRIVA HandiHaler 18 MCG Inhalation Powder
- RxCUI: 580261 - tiotropium 0.018 MG Inhalation Powder [Spiriva]
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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".