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LEVOXYL
LEVOXYL - 60793-859-01 - (LEVOTHYROXINE SODIUM)
Drug Information of LEVOXYL
| Product NDC: | 60793-859 |
| Proprietary Name: | LEVOXYL |
| Non Proprietary Name: | LEVOTHYROXINE SODIUM |
| Active Ingredient(s): | 175 ug/1 & nbsp; LEVOTHYROXINE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of LEVOXYL
| Product NDC: | 60793-859 |
| Labeler Name: | King Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021301 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20010525 |
Package Information of LEVOXYL
| Package NDC: | 60793-859-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (60793-859-01) |
NDC Information of LEVOXYL
| NDC Code | 60793-859-01 |
| Proprietary Name | LEVOXYL |
| Package Description | 100 TABLET in 1 BOTTLE (60793-859-01) |
| Product NDC | 60793-859 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVOTHYROXINE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20010525 |
| Marketing Category Name | NDA |
| Labeler Name | King Pharmaceuticals, Inc. |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | 175 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
