Bumetanide
- Product NDC
- 68071-3128
- 11-digit product format
- 680713128
- Labeler code
- 68071
- Product ID
- 68071-3128_bb134dcd-fa8b-1429-e053-2a95a90a2ada
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-3128-3 | 68071312803 | 30 TABLET in 1 BOTTLE (68071-3128-3) | 30 tablet | 2017-03-23 | 0000-00-00 | No | No | Current |
| 68071-3128-6 | 68071312806 | 60 TABLET in 1 BOTTLE (68071-3128-6) | 60 tablet | 2017-03-23 | 0000-00-00 | No | No | Current |
| 68071-3128-9 | 68071312809 | 90 TABLET in 1 BOTTLE (68071-3128-9) | 90 tablet | 2017-03-23 | 0000-00-00 | No | No | Current |