TORSEMIDE
- Product NDC
- 72189-102
- 11-digit product format
- 721890102
- Labeler code
- 72189
- Product ID
- 72189-102_2be81614-53a3-ed55-e063-6294a90a1152
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- TORSEMIDE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA079234
- Marketing category
- ANDA
- Marketing start
- 2020-05-11
- Substance
- TORSEMIDE
- Active strength
- 10 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 |
|---|
| 72189-102-30 | 72189010230 | 30 TABLET in 1 BOTTLE (72189-102-30) | 30 tablet | 2020-05-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| TORSEMIDE | Direct_Rx | 2025-01-17 | HUMAN PRESCRIPTION DRUG LABEL | 4 |