NDC 16590-279 Uroxatral
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What is NDC 16590-279?
What are the uses for Uroxatral?
Which are Uroxatral UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALFUZOSIN HYDROCHLORIDE (UNII: 75046A1XTN)
- ALFUZOSIN (UNII: 90347YTW5F) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Uroxatral?
- RxCUI: 861132 - alfuzosin HCl 10 MG 24HR Extended Release Oral Tablet
- RxCUI: 861132 - 24 HR alfuzosin hydrochloride 10 MG Extended Release Oral Tablet
- RxCUI: 861132 - alfuzosin hydrochloride 10 MG 24 HR Extended Release Oral Tablet
- RxCUI: 861134 - Uroxatral 10 MG 24HR Extended Release Oral Tablet
- RxCUI: 861134 - 24 HR alfuzosin hydrochloride 10 MG Extended Release Oral Tablet [UroXatral]
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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".