Bumetanide
- Product NDC
- 71335-0016
- 11-digit product format
- 713350016
- Labeler code
- 71335
- Product ID
- 71335-0016_07530a6f-84bf-428e-8f16-813a4dea871b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018225
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-10-15
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- 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 |
|---|
| 71335-0016-1 | 71335001601 | 30 TABLET in 1 BOTTLE (71335-0016-1) | 30 tablet | 2017-10-23 | 0000-00-00 | No | No | Current |
| 71335-0016-2 | 71335001602 | 90 TABLET in 1 BOTTLE (71335-0016-2) | 90 tablet | 2017-10-23 | 0000-00-00 | No | No | Current |
| 71335-0016-3 | 71335001603 | 28 TABLET in 1 BOTTLE (71335-0016-3) | 28 tablet | 2017-10-23 | 0000-00-00 | No | No | Current |
| 71335-0016-4 | 71335001604 | 18 TABLET in 1 BOTTLE (71335-0016-4) | 18 tablet | 2017-10-23 | 0000-00-00 | No | No | Current |