Torsemide
- Product NDC
- 62135-820
- 11-digit product format
- 621350820
- Labeler code
- 62135
- Product ID
- 62135-820_459f249e-79f0-77db-e063-6294a90afda0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Chartwell RX, LLC
- Application
- ANDA076894
- Marketing category
- ANDA
- Marketing start
- 2005-05-31
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Torsemide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TORSEMIDE | 20 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 |
|---|
| 62135-820-90 | Torsemide | 90 in 1 BOTTLE | TABLET | 90 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62135-820 | TORSEMIDE TABLET [CHARTWELL RX, LLC] | 1 | Current NDC, 1 package rows | 20240202_a3d68763-95e0-4ad6-89c2-c4b1c0b43948.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 62135-820-90 | 62135082090 | 90 TABLET in 1 BOTTLE (62135-820-90) | 90 tablet | 2024-01-17 | No | No | Current |