Levothyroxine sodium
- Product NDC
- 68788-8792
- 11-digit product format
- 687888792
- Labeler code
- 68788
- Product ID
- 68788-8792_a55e735f-a5b0-4b85-9fd7-3a4b6723a81b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207588
- Marketing category
- ANDA
- Marketing start
- 2024-12-17
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 88 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 |
|---|
| 68788-8792-3 | 68788879203 | 30 TABLET in 1 BOTTLE (68788-8792-3) | 30 tablet | 2024-12-17 | No | No | Historical |
| 68788-8792-6 | 68788879206 | 90 TABLET in 1 BOTTLE (68788-8792-6) | 90 tablet | 2024-12-17 | No | No | Historical |
| 68788-8792-9 | 68788879209 | 100 TABLET in 1 BOTTLE (68788-8792-9) | 100 tablet | 2024-12-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Preferred Pharmaceuticals Inc. | 2024-12-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |