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Torsemide
Torsemide - 0517-0771-10 - (Torsemide)
Drug Information of Torsemide
| Product NDC: | 0517-0771 |
| Proprietary Name: | Torsemide |
| Non Proprietary Name: | Torsemide |
| Active Ingredient(s): | 10 mg/mL & nbsp; Torsemide |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Torsemide
| Product NDC: | 0517-0771 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090656 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100526 |
Package Information of Torsemide
| Package NDC: | 0517-0771-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0517-0771-10) > 5 mL in 1 VIAL, SINGLE-DOSE (0517-0771-01) |
NDC Information of Torsemide
| NDC Code | 0517-0771-10 |
| Proprietary Name | Torsemide |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0517-0771-10) > 5 mL in 1 VIAL, SINGLE-DOSE (0517-0771-01) |
| Product NDC | 0517-0771 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Torsemide |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100526 |
| Marketing Category Name | ANDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | TORSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
