Levothyroxine sodium
- Product NDC
- 71335-1966
- 11-digit product format
- 713351966
- Labeler code
- 71335
- Product ID
- 71335-1966_b88af5e0-dce3-42bb-9c03-82fe2a6f1c55
- 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
- 88 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 |
|---|
| 71335-1966-1 | 71335196601 | 30 TABLET in 1 BOTTLE (71335-1966-1) | 30 tablet | 2021-09-30 | No | No | Historical |
| 71335-1966-2 | 71335196602 | 90 TABLET in 1 BOTTLE (71335-1966-2) | 90 tablet | 2021-10-06 | No | No | Historical |
| 71335-1966-3 | 71335196603 | 28 TABLET in 1 BOTTLE (71335-1966-3) | 28 tablet | 2024-12-11 | No | No | Historical |
| 71335-1966-4 | 71335196604 | 100 TABLET in 1 BOTTLE (71335-1966-4) | 100 tablet | 2024-12-11 | No | No | Historical |
| 71335-1966-5 | 71335196605 | 60 TABLET in 1 BOTTLE (71335-1966-5) | 60 tablet | 2024-12-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine sodium | Bryant Ranch Prepack | 2024-12-11 | HUMAN PRESCRIPTION DRUG LABEL | 105 |