Torsemide
- Product NDC
- 67296-2190
- 11-digit product format
- 672962190
- Labeler code
- 67296
- Product ID
- 67296-2190_44f2f06d-7bc5-5239-e063-6394a90aac5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA078249
- Marketing category
- ANDA
- Marketing start
- 2007-10-17
- 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 |
|---|
| 67296-2190-3 | 67296219003 | 30 TABLET in 1 BOTTLE (67296-2190-3) | 30 tablet | 2007-10-17 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Torsemide | Redpharm Drug | 2025-12-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |