Levothyroxine sodium
- Product NDC
- 71335-1947
- 11-digit product format
- 713351947
- Labeler code
- 71335
- Product ID
- 71335-1947_61678bc8-f6f2-4640-9e0a-1bb9ffa9633f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2020-11-25
- 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 | 966225 |
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 |
|---|
| 71335-1947-1 | 71335194701 | 30 TABLET in 1 BOTTLE (71335-1947-1) | 30 tablet | 2022-01-13 | 0000-00-00 | No | No | Current |
| 71335-1947-2 | 71335194702 | 100 TABLET in 1 BOTTLE (71335-1947-2) | 100 tablet | 2024-12-11 | 0000-00-00 | No | No | Current |
| 71335-1947-3 | 71335194703 | 90 TABLET in 1 BOTTLE (71335-1947-3) | 90 tablet | 2021-09-14 | 0000-00-00 | No | No | Current |
| 71335-1947-4 | 71335194704 | 60 TABLET in 1 BOTTLE (71335-1947-4) | 60 tablet | 2024-12-11 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Bryant Ranch Prepack | 2024-12-11 | HUMAN PRESCRIPTION DRUG LABEL | 104 |