Levothyroxine Sodium
- Product NDC
- 71205-255
- 11-digit product format
- 712050255
- Labeler code
- 71205
- Product ID
- 71205-255_1e3a3004-3341-47e3-9961-0f8b966c3d1c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021210
- Marketing category
- NDA
- Marketing start
- 2003-12-01
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- .175 mg/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 |
|---|
| 71205-255-30 | 71205025530 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-255-30) | 30 tablet | 2019-04-01 | No | No | Historical |
| 71205-255-60 | 71205025560 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-255-60) | 60 tablet | 2019-04-01 | No | No | Historical |
| 71205-255-90 | 71205025590 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-255-90) | 90 tablet | 2019-04-01 | No | No | Historical |