NDC 53808-1010 Lexiva
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-1010 - Lexiva
Product Characteristics
Product Packages
NDC Code 53808-1010-1
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 53808-1010?
What are the uses for Lexiva?
Which are Lexiva UNII Codes?
The UNII codes for the active ingredients in this product are:
- FOSAMPRENAVIR CALCIUM (UNII: ID1GU2627N)
- AMPRENAVIR (UNII: 5S0W860XNR) (Active Moiety)
Which are Lexiva 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:
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE K30 (UNII: U725QWY32X)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Lexiva?
- RxCUI: 402109 - fosamprenavir calcium 700 MG Oral Tablet
- RxCUI: 402109 - fosamprenavir 700 MG Oral Tablet
- RxCUI: 402109 - fosamprenavir (as fosamprenavir calcium) 700 MG (amprenavir 600 MG) Oral Tablet
- RxCUI: 402110 - Lexiva 700 MG Oral Tablet
- RxCUI: 402110 - fosamprenavir 700 MG Oral Tablet [Lexiva]
* 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".