Liothyronine sodium
- Product NDC
- 71335-2001
- 11-digit product format
- 713352001
- Labeler code
- 71335
- Product ID
- 71335-2001_b72a4a46-952c-47de-9432-b2ff59899e58
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214803
- Marketing category
- ANDA
- Marketing start
- 2021-02-01
- Substance
- LIOTHYRONINE SODIUM
- Active strength
- 5 ug/1
- Pharmacologic classes
- Triiodothyronine [CS], l-Triiodothyronine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| GCA9VV7D2N | LIOTHYRONINE SODIUM | 55-06-1 | LIOTHYRONINE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2001-1 | 71335200101 | 30 TABLET in 1 BOTTLE (71335-2001-1) | 30 tablet | 2022-03-28 | No | No | Historical |
| 71335-2001-2 | 71335200102 | 90 TABLET in 1 BOTTLE (71335-2001-2) | 90 tablet | 2024-09-06 | No | No | Historical |
| 71335-2001-3 | 71335200103 | 60 TABLET in 1 BOTTLE (71335-2001-3) | 60 tablet | 2021-11-29 | No | No | Historical |
| 71335-2001-4 | 71335200104 | 18 TABLET in 1 BOTTLE (71335-2001-4) | 18 tablet | 2024-09-06 | No | No | Historical |
| 71335-2001-5 | 71335200105 | 28 TABLET in 1 BOTTLE (71335-2001-5) | 28 tablet | 2024-09-06 | No | No | Historical |
| 71335-2001-6 | 71335200106 | 100 TABLET in 1 BOTTLE (71335-2001-6) | 100 tablet | 2024-09-06 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Liothyronine sodium | Bryant Ranch Prepack | 2024-09-06 | HUMAN PRESCRIPTION DRUG LABEL | 104 |