Product NDC: | 16590-302 |
Proprietary Name: | LEVOTHYROXINE SODIUM |
Non Proprietary Name: | LEVOTHYROXINE SODIUM |
Active Ingredient(s): | .1 mg/1 & nbsp; LEVOTHYROXINE SODIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-302 |
Labeler Name: | STAT Rx USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021210 |
Marketing Category: | NDA |
Start Marketing Date: | 20031201 |
Package NDC: | 16590-302-90 |
Package Description: | 90 TABLET in 1 BOTTLE (16590-302-90) |
NDC Code | 16590-302-90 |
Proprietary Name | LEVOTHYROXINE SODIUM |
Package Description | 90 TABLET in 1 BOTTLE (16590-302-90) |
Product NDC | 16590-302 |
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 | .1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |