Liothyronine Sodium
- Product NDC
- 71335-9632
- 11-digit product format
- 713359632
- Labeler code
- 71335
- Product ID
- 71335-9632_7e8ca2e4-1c1e-4565-87a1-cd99437d1dac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200295
- Marketing category
- ANDA
- Marketing start
- 2012-12-03
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 50 ug/1
- Pharmacologic classes
- Triiodothyronine [CS], l-Triiodothyronine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Liothyronine Sodium
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LIOTHYRONINE SODIUM | 50 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | GCA9VV7D2N |
| Rxcui | 903703 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-9632-1 | Liothyronine Sodium | 30 in 1 BOTTLE | TABLET | 30 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 71335-9632 | LIOTHYRONINE SODIUM TABLET [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20231109_20cbf84d-80f2-4b94-ad47-6aaa362fb4d0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-9632-1 | 71335963201 | 30 TABLET in 1 BOTTLE (71335-9632-1) | 30 tablet | 2023-01-31 | No | No | Current |