Levothyroxine sodium
- Product NDC
- 71335-2007
- 11-digit product format
- 713352007
- Labeler code
- 71335
- Product ID
- 71335-2007_aff80cf2-0999-4c0d-8ba1-b7e1d0e28ce3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2020-11-25
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 112 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 |
|---|
| 71335-2007-1 | 71335200701 | 30 TABLET in 1 BOTTLE (71335-2007-1) | 30 tablet | 2022-02-25 | No | No | Historical |
| 71335-2007-2 | 71335200702 | 90 TABLET in 1 BOTTLE (71335-2007-2) | 90 tablet | 2022-03-04 | No | No | Historical |
| 71335-2007-3 | 71335200703 | 60 TABLET in 1 BOTTLE (71335-2007-3) | 60 tablet | 2024-12-11 | No | No | Historical |
| 71335-2007-4 | 71335200704 | 18 TABLET in 1 BOTTLE (71335-2007-4) | 18 tablet | 2024-12-11 | No | No | Historical |
| 71335-2007-5 | 71335200705 | 100 TABLET in 1 BOTTLE (71335-2007-5) | 100 tablet | 2023-07-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Bryant Ranch Prepack | 2024-12-11 | HUMAN PRESCRIPTION DRUG LABEL | 103 |