Levothyroxine Sodium
- Product NDC
- 72189-605
- 11-digit product format
- 721890605
- Labeler code
- 72189
- Product ID
- 72189-605_2b361866-e982-567c-e063-6294a90a5a5c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA212399
- Marketing category
- ANDA
- Marketing start
- 2025-01-08
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 112 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 |
|---|
| 72189-605-90 | 72189060590 | 90 TABLET in 1 BOTTLE (72189-605-90) | 90 tablet | 2025-01-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Direct_Rx | 2025-01-08 | HUMAN PRESCRIPTION DRUG LABEL | 1 |