NDC 67544-888 Synthroid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
PURPLE (C48327 - VIOLET)
YELLOW (C48330)
GREEN (C48329 - OLIVE)
RED (C48326 - ROSE)
BROWN (C48332)
SYNTHROID;50
SYNTHROID;75
SYNTHROID;100
SYNTHROID;88
SYNTHROID;112
SYNTHROID;125
Code Structure Chart
Product Details
What is NDC 67544-888?
What are the uses for Synthroid?
Which are Synthroid UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOTHYROXINE SODIUM (UNII: 9J765S329G)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
Which are Synthroid 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:
- ACACIA (UNII: 5C5403N26O)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- TALC (UNII: 7SEV7J4R1U)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 30 (UNII: 2S42T2808B)
What is the NDC to RxNorm Crosswalk for Synthroid?
- RxCUI: 892246 - levothyroxine sodium 100 MCG Oral Tablet
- RxCUI: 892246 - levothyroxine sodium 0.1 MG Oral Tablet
- RxCUI: 892251 - levothyroxine sodium 200 MCG Oral Tablet
- RxCUI: 892251 - levothyroxine sodium 0.2 MG Oral Tablet
- RxCUI: 966158 - SYNTHROID 25 MCG 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".