Liothyronine Sodium
- Product NDC
- 53217-361
- 11-digit product format
- 532170361
- Labeler code
- 53217
- Product ID
- 53217-361_4851a1c6-ffc2-45fe-a849-4e8c4c5eca3c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA200295
- Marketing category
- ANDA
- Marketing start
- 2018-01-11
- Marketing end
- 0000-00-00
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 5 ug/1
- Pharmacologic classes
- l-Triiodothyronine [EPC],Triiodothyronine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 53217-361-30 | Liothyronine Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53217-361 | LIOTHYRONINE SODIUM TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | Legacy NDC, 1 package rows | 20180821_818ae20e-9909-41ec-a0a9-4b6e9e86e794.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53217-361-30 | 53217036130 | 30 in 1 BOTTLE | Historical |