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Torsemide
Torsemide - 59762-1701-1 - (Torsemide)
Drug Information of Torsemide
| Product NDC: | 59762-1701 |
| Proprietary Name: | Torsemide |
| Non Proprietary Name: | Torsemide |
| Active Ingredient(s): | 10 mg/1 & nbsp; Torsemide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Torsemide
| Product NDC: | 59762-1701 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078249 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071017 |
Package Information of Torsemide
| Package NDC: | 59762-1701-1 |
| Package Description: | 100 TABLET in 1 BOTTLE (59762-1701-1) |
NDC Information of Torsemide
| NDC Code | 59762-1701-1 |
| Proprietary Name | Torsemide |
| Package Description | 100 TABLET in 1 BOTTLE (59762-1701-1) |
| Product NDC | 59762-1701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Torsemide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20071017 |
| Marketing Category Name | ANDA |
| Labeler Name | Greenstone LLC |
| Substance Name | TORSEMIDE |
| Strength Number | 10 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC] |
