| Product NDC: | 16590-403 |
| Proprietary Name: | LEVOTHYROXINE SODIUM |
| Non Proprietary Name: | LEVOTHYROXINE SODIUM |
| Active Ingredient(s): | .05 mg/1 & nbsp; LEVOTHYROXINE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 16590-403 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021210 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031201 |
| Package NDC: | 16590-403-82 |
| Package Description: | 180 TABLET in 1 BOTTLE (16590-403-82) |
| NDC Code | 16590-403-82 |
| Proprietary Name | LEVOTHYROXINE SODIUM |
| Package Description | 180 TABLET in 1 BOTTLE (16590-403-82) |
| Product NDC | 16590-403 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVOTHYROXINE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031201 |
| Marketing Category Name | NDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | .05 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |