levothyroxine sodium
- Product NDC
- 71205-352
- 11-digit product format
- 712050352
- Labeler code
- 71205
- Product ID
- 71205-352_3019762c-d480-4530-a3b2-762b523e7961
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021116
- Marketing category
- NDA
- Marketing start
- 2019-05-07
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 50 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 |
|---|
| 71205-352-30 | 71205035230 | 30 TABLET in 1 BOTTLE (71205-352-30) | 30 tablet | 2019-11-01 | No | No | Historical |
| 71205-352-60 | 71205035260 | 60 TABLET in 1 BOTTLE (71205-352-60) | 60 tablet | 2019-11-01 | No | No | Historical |
| 71205-352-90 | 71205035290 | 90 TABLET in 1 BOTTLE (71205-352-90) | 90 tablet | 2019-11-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| levothyroxine sodium | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |