liothyronine sodium
- Product NDC
- 50090-7518
- 11-digit product format
- 500907518
- Labeler code
- 50090
- Product ID
- 50090-7518_be0210a1-cda6-4f01-af18-5b022bbc68a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- liothyronine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091382
- Marketing category
- ANDA
- Marketing start
- 2019-11-28
- 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 |
|---|
| 50090-7518-0 | 50090751800 | 100 TABLET in 1 BOTTLE (50090-7518-0) | 100 tablet | 2025-03-11 | No | No | Historical |
| 50090-7518-1 | 50090751801 | 90 TABLET in 1 BOTTLE (50090-7518-1) | 90 tablet | 2025-03-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| liothyronine sodium | A-S Medication Solutions | 2025-03-12 | Human Prescription Drug Label | 1 |