Levothyroxine Sodium
- Product NDC
- 71335-1940
- 11-digit product format
- 713351940
- Labeler code
- 71335
- Product ID
- 71335-1940_3ba1753b-b511-4832-90e0-2284225e535a
- 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
- 200 ug/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 |
|---|
| 71335-1940-1 | 71335194001 | 100 TABLET in 1 BOTTLE (71335-1940-1) | 100 tablet | 2021-09-10 | No | No | Historical |
| 71335-1940-2 | 71335194002 | 30 TABLET in 1 BOTTLE (71335-1940-2) | 30 tablet | 2021-09-10 | No | No | Historical |
| 71335-1940-3 | 71335194003 | 90 TABLET in 1 BOTTLE (71335-1940-3) | 90 tablet | 2021-09-10 | No | No | Historical |
| 71335-1940-4 | 71335194004 | 60 TABLET in 1 BOTTLE (71335-1940-4) | 60 tablet | 2021-09-10 | No | No | Historical |
| 71335-1940-5 | 71335194005 | 18 TABLET in 1 BOTTLE (71335-1940-5) | 18 tablet | 2021-09-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Bryant Ranch Prepack | 2024-08-21 | HUMAN PRESCRIPTION DRUG LABEL | 107 |