Torsemide
- Product NDC
- 70518-2744
- 11-digit product format
- 705182744
- Labeler code
- 70518
- Product ID
- 70518-2744_ed746c0a-93e1-374a-e053-2a95a90a6337
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA079234
- Marketing category
- ANDA
- Marketing start
- 2020-05-13
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2744 | TORSEMIDE TABLET [REMEDYREPACK INC.] | 7 | Legacy NDC | 20250402_c8081bac-5f4e-4eb0-9099-17e2a519e77a.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2744-0 | 70518274400 | 90 TABLET in 1 BOTTLE, PLASTIC (70518-2744-0) | 90 tablet | 2020-05-13 | 0000-00-00 | No | No | Current |
| 70518-2744-1 | 70518274401 | 30 TABLET in 1 BLISTER PACK (70518-2744-1) | 30 tablet | 2021-08-12 | 0000-00-00 | No | No | Current |