Levothyroxine Sodium
- Product NDC
- 71205-512
- 11-digit product format
- 712050512
- Labeler code
- 71205
- Product ID
- 71205-512_d2f36637-9d33-4514-bec0-81ed87ab79ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-08-03
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 25 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 |
|---|
| 71205-512-30 | 71205051230 | 30 TABLET in 1 BOTTLE (71205-512-30) | 30 tablet | 2020-12-02 | No | No | Historical |
| 71205-512-60 | 71205051260 | 60 TABLET in 1 BOTTLE (71205-512-60) | 60 tablet | 2020-12-02 | No | No | Historical |
| 71205-512-90 | 71205051290 | 90 TABLET in 1 BOTTLE (71205-512-90) | 90 tablet | 2020-12-02 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Proficient Rx LP | 2022-04-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |