Torsemide
- Product NDC
- 71335-0297
- 11-digit product format
- 713350297
- Labeler code
- 71335
- Product ID
- 71335-0297_d54357a9-994d-4ffc-ba07-2f200d48f08c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Torsemide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078249
- Marketing category
- ANDA
- Marketing start
- 2007-10-17
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-0297-1 | 71335029701 | 100 TABLET in 1 BOTTLE (71335-0297-1) | 100 tablet | 2017-08-07 | 0000-00-00 | No | No | Current |
| 71335-0297-2 | 71335029702 | 30 TABLET in 1 BOTTLE (71335-0297-2) | 30 tablet | 2017-08-07 | 0000-00-00 | No | No | Current |
| 71335-0297-3 | 71335029703 | 90 TABLET in 1 BOTTLE (71335-0297-3) | 90 tablet | 2017-08-07 | 0000-00-00 | No | No | Current |