Bumetanide
- Product NDC
- 0615-8394
- 11-digit product format
- 006158394
- Labeler code
- 0615
- Product ID
- 0615-8394_29b20e6a-6c58-4aa8-874a-afb0987a68e2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA209724
- Marketing category
- ANDA
- Marketing start
- 2017-10-18
- 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
- 2022-12-31
- 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 |
|---|
| 0615-8394 | BUMETANIDE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS] | 6 | Legacy NDC | 20241024_e3fa9e19-b82d-4a2b-a471-c2de1f2f5151.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0615-8394-39 | 00615839439 | 30 TABLET in 1 BLISTER PACK (0615-8394-39) | 30 tablet | 2021-05-11 | 0000-00-00 | No | No | Current |