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NDC 68382-0584-10 Liothyronine sodium 50 ug/1 Details
Liothyronine sodium 50 ug/1
Liothyronine sodium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals (USA) Inc.. The primary component is LIOTHYRONINE SODIUM.
MedlinePlus Drug Summary
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.
Related Packages: 68382-0584-10Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Liothyronine
Product Information
| NDC | 68382-0584 |
|---|---|
| Product ID | 68382-584_15ed7dff-a305-4a76-aedd-f932fa27b36c |
| Associated GPIs | 28100020100315 |
| GCN Sequence Number | 006660 |
| GCN Sequence Number Description | liothyronine sodium TABLET 50 MCG ORAL |
| HIC3 | P3A |
| HIC3 Description | THYROID HORMONES |
| GCN | 26342 |
| HICL Sequence Number | 002850 |
| HICL Sequence Number Description | LIOTHYRONINE SODIUM |
| Brand/Generic | Generic |
| Proprietary Name | Liothyronine sodium |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Liothyronine sodium |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 50 |
| Active Ingredient Units | ug/1 |
| Substance Name | LIOTHYRONINE SODIUM |
| Labeler Name | Zydus Pharmaceuticals (USA) Inc. |
| Pharmaceutical Class | Triiodothyronine [CS], l-Triiodothyronine [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA214803 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68382-0584-10 (68382058410)
| NDC Package Code | 68382-584-10 |
|---|---|
| Billing NDC | 68382058410 |
| Package | 1000 TABLET in 1 BOTTLE (68382-584-10) |
| Marketing Start Date | 2021-02-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |