Levothyroxine sodium
- Product NDC
- 71205-642
- 11-digit product format
- 712050642
- Labeler code
- 71205
- Product ID
- 71205-642_7a6abcab-a753-4c1d-92fb-c134ffc2c0a7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2020-12-10
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 100 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 |
|---|
| 71205-642-30 | 71205064230 | 30 TABLET in 1 BOTTLE (71205-642-30) | 30 tablet | 2022-03-10 | No | No | Historical |
| 71205-642-60 | 71205064260 | 60 TABLET in 1 BOTTLE (71205-642-60) | 60 tablet | 2022-03-10 | No | No | Historical |
| 71205-642-90 | 71205064290 | 90 TABLET in 1 BOTTLE (71205-642-90) | 90 tablet | 2022-03-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Proficient Rx LP | 2022-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |