Levothyroxine Sodium
- Product NDC
- 68071-3787
- 11-digit product format
- 680713787
- Labeler code
- 68071
- Product ID
- 68071-3787_2cf49703-3f83-f503-e063-6394a90a61f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Levothyroxine Sodium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA209713
- Marketing category
- ANDA
- Marketing start
- 2019-03-20
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- .2 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 |
|---|
| 68071-3787-9 | 68071378709 | 90 TABLET in 1 BOTTLE (68071-3787-9) | 90 tablet | 2025-01-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Levothyroxine Sodium | NuCare Pharmaceuticals, Inc. | 2025-01-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |