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UNITHROID
UNITHROID - 0527-1639-01 - (levothyroxine sodium)
Drug Information of UNITHROID
| Product NDC: | 0527-1639 |
| Proprietary Name: | UNITHROID |
| Non Proprietary Name: | levothyroxine sodium |
| Active Ingredient(s): | .137 mg/1 & nbsp; levothyroxine sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of UNITHROID
| Product NDC: | 0527-1639 |
| Labeler Name: | Lannett Company, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021210 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20071001 |
Package Information of UNITHROID
| Package NDC: | 0527-1639-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (0527-1639-01) |
NDC Information of UNITHROID
| NDC Code | 0527-1639-01 |
| Proprietary Name | UNITHROID |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (0527-1639-01) |
| Product NDC | 0527-1639 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | levothyroxine sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071001 |
| Marketing Category Name | NDA |
| Labeler Name | Lannett Company, Inc. |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | .137 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
