levothyroxine sodium
- Product NDC
- 71335-1512
- 11-digit product format
- 713351512
- Labeler code
- 71335
- Product ID
- 71335-1512_5dd258ee-53fd-4e60-b3c9-b3cfacd622bf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021116
- Marketing category
- NDA
- Marketing start
- 2019-05-07
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 150 ug/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 | 150 ug/1 |
Harmonized Identifiers
| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 892246, 892251, 966220, 966221, 966222, 966224, 966225, 966248, 966249, 966253, 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 |
|---|
| 71335-1512-1 | 71335151201 | 30 TABLET in 1 BOTTLE (71335-1512-1) | 30 tablet | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1512-2 | 71335151202 | 100 TABLET in 1 BOTTLE (71335-1512-2) | 100 tablet | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1512-3 | 71335151203 | 90 TABLET in 1 BOTTLE (71335-1512-3) | 90 tablet | 2020-02-18 | 0000-00-00 | No | No | Current |
| 71335-1512-4 | 71335151204 | 60 TABLET in 1 BOTTLE (71335-1512-4) | 60 tablet | 2020-02-18 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| levothyroxine sodium | Bryant Ranch Prepack | 2025-07-29 | HUMAN PRESCRIPTION DRUG LABEL | 26 |