bumetanide
- Product NDC
- 0615-8362
- 11-digit product format
- 006158362
- Labeler code
- 0615
- Product ID
- 0615-8362_1e08f71d-8e83-492e-9b97-0f14e0b2f1b8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA074225
- Marketing category
- ANDA
- Marketing start
- 2019-06-01
- Marketing end
- 2022-09-30
- 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
- 0000-00-00
- 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 |
|---|
| 0615-8362-39 | 00615836239 | 30 TABLET in 1 BLISTER PACK (0615-8362-39) | 30 tablet | 2020-11-11 | 2022-09-30 | No | No | Current |