NDC 51655-122 Liothyronine Sodium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51655 - Northwind Pharmaceuticals
- 51655-122 - Liothyronine Sodium
Product Characteristics
Product Packages
NDC Code 51655-122-52
Package Description: 30 TABLET in 1 BOTTLE, DISPENSING
Product Details
What is NDC 51655-122?
What are the uses for Liothyronine Sodium?
Which are Liothyronine Sodium UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIOTHYRONINE SODIUM (UNII: GCA9VV7D2N)
- LIOTHYRONINE (UNII: 06LU7C9H1V) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Liothyronine Sodium?
- RxCUI: 903703 - liothyronine sodium 50 MCG Oral Tablet
- RxCUI: 903703 - liothyronine sodium 0.05 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Liothyronine
Liothyronine is used to treat hypothyroidism (a condition where the thyroid gland does not produce enough thyroid hormone). Liothyronine is also used to treat a goiter (an enlarged thyroid gland) and to test for hyperthyroidism (a condition where the thyroid gland produces too much thyroid hormone). Liothyronine is in a class of medications called thyroid agents. It works by supplying the thyroid hormones normally produced by the body. Currently, there is not enough evidence from clinical studies to support the use of liothyronine, alone or in combination with other medications, as the first choice of therapy to treat hypothyroidism.
[Learn More]
* 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".