NDC 54868-5046 Uroxatral
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 54868-5046?
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)
Which are Uroxatral 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLCELLULOSE (100 MPA.S) (UNII: 47MLB0F1MV)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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".