Product NDC: | 0517-0770 |
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) |
Product NDC: | 0517-0770 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090656 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100521 |
Package NDC: | 0517-0770-10 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0517-0770-10) > 2 mL in 1 VIAL, SINGLE-DOSE (0517-0770-01) |
NDC Code | 0517-0770-10 |
Proprietary Name | Torsemide |
Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0517-0770-10) > 2 mL in 1 VIAL, SINGLE-DOSE (0517-0770-01) |
Product NDC | 0517-0770 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Torsemide |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20100521 |
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] |