Bumetanide
- Product NDC
- 43353-292
- 11-digit product format
- 433530292
- Labeler code
- 43353
- Product ID
- 43353-292_b3048e2b-3ff7-4160-870f-147d792ec36c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 43353-292 | BUMETANIDE TABLET [APHENA PHARMA SOLUTIONS - TENNESSEE, LLC] | 2 | Legacy NDC | 20171024_4b1181a4-d456-40b8-9434-8f8a99238324.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43353-292-51 | 43353029251 | 6000 TABLET in 1 BOTTLE (43353-292-51) | 6000 tablet | 2017-03-10 | 0000-00-00 | No | No | Current |