levothyroxine sodium
- Product NDC
- 72162-1460
- 11-digit product format
- 721621460
- Labeler code
- 72162
- Product ID
- 72162-1460_0f6ff30f-796d-40a7-b876-bfa12a273e7c
- 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
- 75 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 |
|---|
| 72162-1460-0 | 72162146000 | 1000 TABLET in 1 BOTTLE (72162-1460-0) | 1000 tablet | 2024-01-05 | No | No | Historical |
| 72162-1460-3 | 72162146003 | 30 TABLET in 1 BOTTLE (72162-1460-3) | 30 tablet | 2024-01-05 | No | No | Historical |
| 72162-1460-6 | 72162146006 | 60 TABLET in 1 BOTTLE (72162-1460-6) | 60 tablet | 2024-01-05 | No | No | Historical |
| 72162-1460-9 | 72162146009 | 90 TABLET in 1 BOTTLE (72162-1460-9) | 90 tablet | 2024-01-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| levothyroxine sodium | Bryant Ranch Prepack | 2025-01-21 | HUMAN PRESCRIPTION DRUG LABEL | 102 |