Torsemide
- Product NDC
- 71335-2841
- 11-digit product format
- 713352841
- Labeler code
- 71335
- Product ID
- 71335-2841_127e6c86-1d66-461a-9c8b-df9e7e63034b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076894
- Marketing category
- ANDA
- Marketing start
- 2023-07-24
- 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 |
|---|
| 71335-2841-1 | 71335284101 | 100 TABLET in 1 BOTTLE (71335-2841-1) | 100 tablet | 2025-10-22 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Torsemide | Bryant Ranch Prepack | 2025-10-22 | HUMAN PRESCRIPTION DRUG LABEL | 100 |