NDC 53808-0679 Levothyroxine Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0679 - Levothyroxine Sodium
Product Characteristics
GRAY (C48324)
BLUE (C48333)
M;L;10
M;L;11
Product Packages
NDC Code 53808-0679-1
Package Description: 30 TABLET in 1 BLISTER PACK
Product Details
What is NDC 53808-0679?
What are the uses for Levothyroxine Sodium?
Which are Levothyroxine Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVOTHYROXINE SODIUM (UNII: 9J765S329G)
- LEVOTHYROXINE (UNII: Q51BO43MG4) (Active Moiety)
Which are Levothyroxine Sodium 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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MANNITOL (UNII: 3OWL53L36A)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SUCROSE (UNII: C151H8M554)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Levothyroxine Sodium?
- RxCUI: 966222 - levothyroxine sodium 75 MCG Oral Tablet
- RxCUI: 966222 - levothyroxine sodium 0.075 MG Oral Tablet
- RxCUI: 966224 - levothyroxine sodium 125 MCG Oral Tablet
- RxCUI: 966224 - levothyroxine sodium 0.125 MG Oral Tablet
- RxCUI: 966225 - levothyroxine sodium 150 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".