levothyroxine sodium
- Product NDC
- 71335-1502
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021116
- Marketing category
- NDA
- Substance
- LEVOTHYROXINE SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71335-1502-1 | 30 TABLET in 1 BOTTLE (71335-1502-1) | 2020-02-24 | | No | Historical |
| 71335-1502-2 | 90 TABLET in 1 BOTTLE (71335-1502-2) | 2024-04-09 | | No | Historical |
| 71335-1502-3 | 100 TABLET in 1 BOTTLE (71335-1502-3) | 2020-02-24 | | No | Historical |
| 71335-1502-4 | 7 TABLET in 1 BOTTLE (71335-1502-4) | 2020-02-24 | | No | Historical |
| 71335-1502-5 | 14 TABLET in 1 BOTTLE (71335-1502-5) | 2020-02-24 | | No | Historical |
| 71335-1502-6 | 60 TABLET in 1 BOTTLE (71335-1502-6) | 2020-02-24 | | No | Historical |
| 71335-1502-7 | 21 TABLET in 1 BOTTLE (71335-1502-7) | 2020-02-24 | | No | Historical |
| 71335-1502-8 | 42 TABLET in 1 BOTTLE (71335-1502-8) | 2020-02-24 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| levothyroxine sodium | Bryant Ranch Prepack | 2025-07-29 | HUMAN PRESCRIPTION DRUG LABEL | 26 |