Torsemide
- Product NDC
- 50111-918
- 11-digit product format
- 501110918
- Labeler code
- 50111
- Product ID
- 50111-918_4ff14943-97b8-4b1c-8600-95c1e3540008
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA076346
- Marketing category
- ANDA
- Marketing start
- 2004-10-20
- Substance
- TORSEMIDE
- Active strength
- 100 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Torsemide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TORSEMIDE | 100 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | W31X2H97FB |
| Rxcui | 198369, 198370, 198371, 198372 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50111-918-01 | Torsemide | 100 in 1 BOTTLE | TABLET | 100 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50111-918 | TORSEMIDE TABLET [TEVA PHARMACEUTICALS USA, INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20211028_8a95cbdb-0601-47a5-9b3a-0c3b0629ceb9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50111-918-01 | 50111091801 | 100 TABLET in 1 BOTTLE (50111-918-01) | 100 tablet | 2004-10-20 | 0000-00-00 | No | No | Current |