NDC 54868-5312 Levothroid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5312 - Levothroid
Product Characteristics
PURPLE (C48327 - LILAC)
PINK (C48328 - PINK)
175;T4
200;T4
Product Packages
NDC Code 54868-5312-0
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5312-1
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-5312-2
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5312?
What are the uses for Levothroid?
Which are Levothroid UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOTHYROXINE SODIUM (UNII: 9J765S329G)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
Which are Levothroid 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)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE K29/32 (UNII: 390RMW2PEQ)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Levothroid?
- RxCUI: 892251 - levothyroxine sodium 200 MCG Oral Tablet
- RxCUI: 892251 - levothyroxine sodium 0.2 MG Oral Tablet
- RxCUI: 966199 - Levothroid 150 MCG Oral Tablet
- RxCUI: 966199 - levothyroxine sodium 0.15 MG Oral Tablet [Levothroid]
- RxCUI: 966199 - Levothroid 0.15 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".