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Demadex
Demadex - 54868-4687-3 - (Torsemide)
Drug Information of Demadex
| 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) |
Labeler Information of Demadex
| 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 Information of Demadex
| Package NDC: | 54868-4687-3 |
| Package Description: | 90 TABLET in 1 BOTTLE (54868-4687-3) |
NDC Information of Demadex
| NDC Code | 54868-4687-3 |
| Proprietary Name | Demadex |
| Package Description | 90 TABLET in 1 BOTTLE (54868-4687-3) |
| 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] |
