LEVOTHYROXINE SODIUM
- Product NDC
- 68071-3887
- 11-digit product format
- 680713887
- Labeler code
- 68071
- Product ID
- 68071-3887_47cfe577-b4ca-d35e-e063-6394a90ad8c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA211417
- Marketing category
- ANDA
- Marketing start
- 2025-04-08
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 75 ug/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LEVOTHYROXINE SODIUM
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LEVOTHYROXINE SODIUM | 75 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 966222 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68071-3887-3 | LEVOTHYROXINE SODIUM | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 68071-3887-9 | LEVOTHYROXINE SODIUM | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3887-3 | 68071388703 | 30 TABLET in 1 BOTTLE (68071-3887-3) | 30 tablet | 2026-01-07 | No | No | Historical |
| 68071-3887-9 | 68071388709 | 90 TABLET in 1 BOTTLE (68071-3887-9) | 90 tablet | 2025-08-28 | No | No | Historical |