LEVOTHYROXINE SODIUM
- Product NDC
- 50090-7562
- 11-digit product format
- 500907562
- Labeler code
- 50090
- Product ID
- 50090-7562_a65719a2-b274-4266-9d37-401d390f86a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA211417
- Marketing category
- ANDA
- Marketing start
- 2025-04-08
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 50 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 |
|---|
| 50090-7562-0 | 50090756200 | 30 TABLET in 1 BOTTLE (50090-7562-0) | 30 tablet | 2025-05-28 | No | No | Historical |
| 50090-7562-1 | 50090756201 | 90 TABLET in 1 BOTTLE (50090-7562-1) | 90 tablet | 2025-05-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LEVOTHYROXINE SODIUM | A-S Medication Solutions | 2025-05-30 | Human Prescription Drug Label | 1 |