Liothyronine Sodium
- Product NDC
- 68071-3571
- 11-digit product format
- 680713571
- Labeler code
- 68071
- Product ID
- 68071-3571_1133ebe8-38c3-2505-e063-6294a90aaa2f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Liothyronine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200295
- Marketing category
- ANDA
- Marketing start
- 2012-12-03
- 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 |
|---|
| 68071-3571-9 | 68071357109 | 90 TABLET in 1 BOTTLE (68071-3571-9) | 90 tablet | 2024-02-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Liothyronine Sodium | NuCare Pharmaceuticals,Inc. | 2024-02-12 | HUMAN PRESCRIPTION DRUG LABEL | 1 |