Levothyroxine sodium
- Product NDC
- 68788-8902
- 11-digit product format
- 687888902
- Labeler code
- 68788
- Product ID
- 68788-8902_64aaeba7-1013-44a4-96fc-b876016897b3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA207588
- Marketing category
- ANDA
- Marketing start
- 2025-07-25
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 200 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 |
|---|
| 68788-8902-3 | 68788890203 | 30 TABLET in 1 BOTTLE (68788-8902-3) | 30 tablet | 2025-07-25 | No | No | Historical |
| 68788-8902-9 | 68788890209 | 90 TABLET in 1 BOTTLE (68788-8902-9) | 90 tablet | 2025-07-25 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Preferred Pharmaceuticals Inc. | 2025-07-25 | HUMAN PRESCRIPTION DRUG LABEL | 1 |