Product NDC: | 54868-4687 |
Proprietary Name: | Demadex |
Non Proprietary Name: | Torsemide |
Active Ingredient(s): | 20 mg/1 & nbsp; Torsemide |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-4687 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020136 |
Marketing Category: | NDA |
Start Marketing Date: | 20091021 |
Package NDC: | 54868-4687-1 |
Package Description: | 10 TABLET in 1 BOTTLE (54868-4687-1) |
NDC Code | 54868-4687-1 |
Proprietary Name | Demadex |
Package Description | 10 TABLET in 1 BOTTLE (54868-4687-1) |
Product NDC | 54868-4687 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Torsemide |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20091021 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | TORSEMIDE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |