Levothyroxine Sodium
- Product NDC
- 70518-4390
- 11-digit product format
- 705184390
- Labeler code
- 70518
- Product ID
- 70518-4390_3a0f1dcd-e74d-b7a2-e063-6394a90a08cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA209713
- Marketing category
- ANDA
- Marketing start
- 2025-07-14
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- .05 mg/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 |
|---|
| 70518-4390-0 | 70518439000 | 90 TABLET in 1 BOTTLE (70518-4390-0) | 90 tablet | 2025-07-14 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | REMEDYREPACK INC. | 2025-07-16 | HUMAN PRESCRIPTION DRUG LABEL | 2 |