NDC 53808-0958 Synthroid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0958 - Synthroid
Product Characteristics
Product Packages
NDC Code 53808-0958-2
Package Description: 60 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0958?
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)
- TALC (UNII: 7SEV7J4R1U)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- POVIDONES (UNII: FZ989GH94E)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Synthroid?
- RxCUI: 966171 - SYNTHROID 75 MCG Oral Tablet
- RxCUI: 966171 - levothyroxine sodium 0.075 MG Oral Tablet [Synthroid]
- RxCUI: 966171 - Synthroid 0.075 MG Oral Tablet
- RxCUI: 966171 - Synthroid 75 MCG Oral Tablet
- RxCUI: 966222 - levothyroxine sodium 75 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".