NDC 54868-4801 Doxazosin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4801 - Doxazosin
Product Characteristics
PINK (C48328)
M;D10
Product Packages
NDC Code 54868-4801-0
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4801-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4801-2
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-4801-3
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4801?
What are the uses for Doxazosin?
Which are Doxazosin UNII Codes?
The UNII codes for the active ingredients in this product are:
- DOXAZOSIN MESYLATE (UNII: 86P6PQK0MU)
- DOXAZOSIN (UNII: NW1291F1W8) (Active Moiety)
Which are Doxazosin 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- D&C RED NO. 30 (UNII: 2S42T2808B)
What is the NDC to RxNorm Crosswalk for Doxazosin?
- RxCUI: 197625 - doxazosin mesylate 1 MG Oral Tablet
- RxCUI: 197625 - doxazosin 1 MG Oral Tablet
- RxCUI: 197625 - doxazosin (as doxazosin mesylate) 1 MG Oral Tablet
- RxCUI: 197626 - doxazosin mesylate 2 MG Oral Tablet
- RxCUI: 197626 - doxazosin 2 MG 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".