NDC 54868-4534 Levoxyl
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4534 - Levoxyl
Product Characteristics
WHITE (C48325)
PURPLE (C48327)
LEVOXYL;DP;50
LEVOXYL;DP;75
Product Packages
NDC Code 54868-4534-1
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 54868-4534-2
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 54868-4534?
What are the uses for Levoxyl?
Which are Levoxyl UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOTHYROXINE SODIUM (UNII: 9J765S329G)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
Which are Levoxyl 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CALCIUM SULFATE DIHYDRATE (UNII: 4846Q921YM)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 30 (UNII: 2S42T2808B)
What is the NDC to RxNorm Crosswalk for Levoxyl?
- RxCUI: 892246 - levothyroxine sodium 100 MCG Oral Tablet
- RxCUI: 892246 - levothyroxine sodium 0.1 MG Oral Tablet
- RxCUI: 966157 - LEVOXYL 25 MCG Oral Tablet
- RxCUI: 966157 - levothyroxine sodium 0.025 MG Oral Tablet [Levoxyl]
- RxCUI: 966157 - Levoxyl 0.025 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".