Levothyroxine Sodium
- Product NDC
- 43063-950
- 11-digit product format
- 430630950
- Labeler code
- 43063
- Product ID
- 43063-950_d2bf159f-e140-538f-e053-2a95a90ae5e0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- NDA021210
- Marketing category
- NDA
- Marketing start
- 2003-12-01
- Marketing end
- 0000-00-00
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 0 mg/1
- Pharmacologic classes
- l-Thyroxine [EPC],Thyroxine [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-950-90 | 43063095090 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-950-90) | 90 tablet | 2019-02-21 | 0000-00-00 | No | No | Current |