NDC 50090-4414 Spiriva
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What is NDC 50090-4414?
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)
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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Patient Education
Tiotropium Oral Inhalation
Tiotropium is used to prevent wheezing, shortness of breath, coughing, and chest tightness in patients with chronic obstructive pulmonary disease (COPD, a group of diseases that affect the lungs and airways) such as chronic bronchitis (swelling of the air passages that lead to the lungs) and emphysema (damage to air sacs in the lungs). Tiotropium is in a class of medications called bronchodilators. It works by relaxing and opening the air passages to the lungs to make breathing easier.
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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".