NDC 54868-2271 Levothyroxine Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
TURQUOISE (C48334)
BLUE (C48333)
PURPLE (C48327 - LILAC)
PINK (C48328)
GREEN (C48329)
M;L;15
M;L;11
M;L;12
M;L;13
M;L;14
Code Structure Chart
Product Details
What is NDC 54868-2271?
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. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- D&C RED NO. 27 (UNII: 2LRS185U6K)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Levothyroxine Sodium?
- RxCUI: 892251 - levothyroxine sodium 200 MCG Oral Tablet
- RxCUI: 892251 - levothyroxine sodium 0.2 MG Oral Tablet
- RxCUI: 892255 - levothyroxine sodium 300 MCG Oral Tablet
- RxCUI: 892255 - levothyroxine sodium 0.3 MG Oral Tablet
- RxCUI: 966224 - levothyroxine sodium 125 MCG Oral Tablet
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[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".