Levothyroxine Sodium
- Product NDC
- 68071-3750
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA209713
- Marketing category
- ANDA
- Substance
- LEVOTHYROXINE SODIUM
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3750-9 | 90 TABLET in 1 BOTTLE (68071-3750-9) | 2024-12-20 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | NuCare Pharmaceuticals,Inc. | 2024-12-20 | HUMAN PRESCRIPTION DRUG LABEL | 1 |