NDC 43353-746 Alfuzosin Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-746 - Alfuzosin Hydrochloride
Product Characteristics
Product Packages
NDC Code 43353-746-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-746-60
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-746?
What are the uses for Alfuzosin Hydrochloride?
Which are Alfuzosin Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALFUZOSIN HYDROCHLORIDE (UNII: 75046A1XTN)
- ALFUZOSIN (UNII: 90347YTW5F) (Active Moiety)
Which are Alfuzosin Hydrochloride 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:
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POVIDONES (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Alfuzosin Hydrochloride?
- 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
* Please review the disclaimer below.
[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".