LEVOTHYROXINE SODIUM
- Product NDC
- 68788-8806
- 11-digit product format
- 687888806
- Labeler code
- 68788
- Product ID
- 68788-8806_7ade3f9e-e3d2-401b-a6b7-aa4c9d1c9861
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- LEVOTHYROXINE SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA211417
- Marketing category
- ANDA
- Marketing start
- 2025-01-20
- Substance
- LEVOTHYROXINE SODIUM
- Active strength
- 75 ug/1
- Pharmacologic classes
- Thyroxine [CS], l-Thyroxine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- LEVOTHYROXINE SODIUM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| LEVOTHYROXINE SODIUM | 75 ug/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 9J765S329G |
| Rxcui | 892246, 966222, 966249 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8806-3 | 68788880603 | 30 TABLET in 1 BOTTLE (68788-8806-3) | 30 tablet | 2025-01-20 | No | No | Historical |
| 68788-8806-9 | 68788880609 | 90 TABLET in 1 BOTTLE (68788-8806-9) | 90 tablet | 2025-01-20 | No | No | Historical |