Levothyroxine Sodium
- Product NDC
- 71335-2289
- 11-digit product format
- 713352289
- Labeler code
- 71335
- Product ID
- 71335-2289_e20a1ae7-751d-464c-88cb-d830cbbbe678
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA021342
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-08-03
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 75 ug/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 71335-2289-1 | 71335228901 | 1000 TABLET in 1 BOTTLE (71335-2289-1) | 1000 tablet | 2024-04-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Bryant Ranch Prepack | 2026-05-15 | HUMAN PRESCRIPTION DRUG LABEL | 102 |