Torsemide
- Product NDC
- 71610-819
- 11-digit product format
- 716100819
- Labeler code
- 71610
- Product ID
- 71610-819_159e8c9e-1f33-0a23-e063-6394a90abc74
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA076943
- Marketing category
- ANDA
- Marketing start
- 2005-03-01
- Substance
- TORSEMIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W31X2H97FB | TORSEMIDE | 56211-40-6 | TORSEMIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71610-819-22 | 71610081922 | 1170 TABLET in 1 BOTTLE (71610-819-22) | 1170 tablet | 2024-04-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Torsemide | Aphena Pharma Solutions - Tennessee, LLC | 2024-04-08 | HUMAN PRESCRIPTION DRUG LABEL | 1 |