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Cytomel
Cytomel - 54868-1750-0 - (liothyronine sodium)
Drug Information of Cytomel
| Product NDC: | 54868-1750 |
| Proprietary Name: | Cytomel |
| Non Proprietary Name: | liothyronine sodium |
| Active Ingredient(s): | 25 ug/1 & nbsp; liothyronine sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytomel
| Product NDC: | 54868-1750 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA010379 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20021230 |
Package Information of Cytomel
| Package NDC: | 54868-1750-0 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (54868-1750-0) |
NDC Information of Cytomel
| NDC Code | 54868-1750-0 |
| Proprietary Name | Cytomel |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (54868-1750-0) |
| Product NDC | 54868-1750 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | liothyronine sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20021230 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | LIOTHYRONINE SODIUM |
| Strength Number | 25 |
| Strength Unit | ug/1 |
| Pharmaceutical Classes | l-Triiodothyronine [EPC],Triiodothyronine [Chemical/Ingredient] |
