Levothyroxine Sodium
- Product NDC
- 71205-237
- 11-digit product format
- 712050237
- Labeler code
- 71205
- Product ID
- 71205-237_98d19b29-166e-42ae-ae3b-1ad981327766
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- NDA021210
- Marketing category
- NDA
- Marketing start
- 2007-10-01
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- .137 mg/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data
- Finished product
- Yes
- Brand name base
- Levothyroxine Sodium
- Listing expiration
- 2026-12-31
Active Ingredients
| Ingredient | Strength |
|---|
| LEVOTHYROXINE SODIUM | .137 mg/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 966270 |
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 71205-237-30 | 71205023730 | 30 TABLET in 1 BOTTLE, PLASTIC (71205-237-30) | 30 tablet | 2019-03-01 | 0000-00-00 | No | No | Current |
| 71205-237-60 | 71205023760 | 60 TABLET in 1 BOTTLE, PLASTIC (71205-237-60) | 60 tablet | 2019-03-01 | 0000-00-00 | No | No | Current |
| 71205-237-90 | 71205023790 | 90 TABLET in 1 BOTTLE, PLASTIC (71205-237-90) | 90 tablet | 2019-03-01 | 0000-00-00 | No | No | Current |