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Thyrolar
Thyrolar - 0456-0060-01 - (liothyronine sodium, LEVOTHYROXINE SODIUM)
Drug Information of Thyrolar
| Product NDC: | 0456-0060 |
| Proprietary Name: | Thyrolar |
| Non Proprietary Name: | liothyronine sodium, LEVOTHYROXINE SODIUM |
| Active Ingredient(s): | 150; 37.5 ug/1; ug/1 & nbsp; liothyronine sodium, LEVOTHYROXINE SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Thyrolar
| Product NDC: | 0456-0060 |
| Labeler Name: | Forest Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA016807 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19691121 |
Package Information of Thyrolar
| Package NDC: | 0456-0060-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0456-0060-01) |
NDC Information of Thyrolar
| NDC Code | 0456-0060-01 |
| Proprietary Name | Thyrolar |
| Package Description | 100 TABLET in 1 BOTTLE (0456-0060-01) |
| Product NDC | 0456-0060 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | liothyronine sodium, LEVOTHYROXINE SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19691121 |
| Marketing Category Name | NDA |
| Labeler Name | Forest Laboratories, Inc |
| Substance Name | LEVOTHYROXINE SODIUM; LIOTHYRONINE SODIUM |
| Strength Number | 150; 37.5 |
| Strength Unit | ug/1; ug/1 |
| Pharmaceutical Classes | l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient],l-Thyroxine [EPC],Thyroxine [Chemical/Ingredient] |
