levothyroxine sodium
- Product NDC
- 71205-543
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021116
- Marketing category
- NDA
- Substance
- LEVOTHYROXINE SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-543-30 | 30 TABLET in 1 BOTTLE (71205-543-30) | 2021-03-10 | | No | Historical |
| 71205-543-60 | 60 TABLET in 1 BOTTLE (71205-543-60) | 2021-03-10 | | No | Historical |
| 71205-543-90 | 90 TABLET in 1 BOTTLE (71205-543-90) | 2021-03-10 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| levothyroxine sodium | Proficient Rx LP | 2021-03-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |