Torsemide
- Product NDC
- 70518-4139
- 11-digit product format
- 705184139
- Labeler code
- 70518
- Product ID
- 70518-4139_3fb3d974-66dd-abd2-e063-6294a90a4f4b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076894
- Marketing category
- ANDA
- Marketing start
- 2024-07-11
- 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 | 198371 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4139-0 | Torsemide | 30 in 1 BLISTER PACK | TABLET | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4139 | TORSEMIDE TABLET [REMEDYREPACK INC.] | 1 | Current NDC, 1 package rows | 20240716_26a3af16-39fc-482d-8a8e-9473af4b0e3f.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 |
|---|
| 70518-4139-0 | 70518413900 | 30 TABLET in 1 BLISTER PACK (70518-4139-0) | 30 tablet | 2024-07-11 | No | No | Current |