LEVOTHYROXINE SODIUM
- Product NDC
- 70518-4434
- 11-digit product format
- 705184434
- Labeler code
- 70518
- Product ID
- 70518-4434_3c30c4bd-3c23-5be4-e063-6294a90a9392
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA211417
- Marketing category
- ANDA
- Marketing start
- 2025-08-12
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 88 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 |
|---|
| 70518-4434-0 | 70518443400 | 90 TABLET in 1 BOTTLE (70518-4434-0) | 90 tablet | 2025-08-12 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| LEVOTHYROXINE SODIUM | REMEDYREPACK INC. | 2025-08-12 | HUMAN PRESCRIPTION DRUG LABEL | 1 |