Levothyroxine Sodium
- Product NDC
- 72162-1092
- 11-digit product format
- 721621092
- Labeler code
- 72162
- Product ID
- 72162-1092_d6ce9798-7204-41df-9aeb-067000cb0895
- 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
- 137 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 |
|---|
| 72162-1092-0 | 72162109200 | 1000 TABLET in 1 BOTTLE (72162-1092-0) | 1000 tablet | 2020-08-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Bryant Ranch Prepack | 2024-04-05 | HUMAN PRESCRIPTION DRUG LABEL | 101 |