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Levothroid
Levothroid - 0456-1321-01 - (LEVOTHYROXINE SODIUM)
Drug Information of Levothroid
| Product NDC: | 0456-1321 |
| Proprietary Name: | Levothroid |
| Non Proprietary Name: | LEVOTHYROXINE SODIUM |
| Active Ingredient(s): | 50 ug/1 & nbsp; LEVOTHYROXINE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Levothroid
| Product NDC: | 0456-1321 |
| Labeler Name: | Forest Laboratories, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021116 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20031016 |
Package Information of Levothroid
| Package NDC: | 0456-1321-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0456-1321-01) |
NDC Information of Levothroid
| NDC Code | 0456-1321-01 |
| Proprietary Name | Levothroid |
| Package Description | 100 TABLET in 1 BOTTLE (0456-1321-01) |
| Product NDC | 0456-1321 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | LEVOTHYROXINE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20031016 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc. |
| Substance Name | LEVOTHYROXINE SODIUM |
| Strength Number | 50 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
