Levothyroxine sodium
- Product NDC
- 68788-7929
- 11-digit product format
- 687887929
- Labeler code
- 68788
- Product ID
- 68788-7929_1b66f796-ddcc-4fc5-8dc2-d45a62ec63cd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2021-06-15
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 100 ug/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [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 |
|---|
| 9J765S329G | LEVOTHYROXINE SODIUM | 6106-07-6 | LEVOTHYROXINE SODIUM |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-7929-1 | 68788792901 | 100 TABLET in 1 BOTTLE (68788-7929-1) | 100 tablet | 2021-06-15 | No | No | Historical |
| 68788-7929-3 | 68788792903 | 30 TABLET in 1 BOTTLE (68788-7929-3) | 30 tablet | 2021-06-15 | No | No | Historical |
| 68788-7929-9 | 68788792909 | 90 TABLET in 1 BOTTLE (68788-7929-9) | 90 tablet | 2021-06-15 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Preferred Pharmaceuticals Inc. | 2025-07-15 | HUMAN PRESCRIPTION DRUG LABEL | 5 |