Levothyroxine Sodium
- Product NDC
- 55154-4377
- 11-digit product format
- 551544377
- Labeler code
- 55154
- Product ID
- 55154-4377_775eb495-e0b3-4922-a17e-092ae8394cda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- levothyroxine sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- Application
- ANDA076187
- Marketing category
- ANDA
- Marketing start
- 2007-02-26
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 150 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 |
|---|
| 55154-4377-0 | 55154437700 | 10 BLISTER PACK in 1 BAG (55154-4377-0) / 1 TABLET in 1 BLISTER PACK | 10 blister pack | 2010-10-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | Cardinal Health 107, LLC | 2025-01-27 | HUMAN PRESCRIPTION DRUG LABEL | 24 |