Bumetanide
- Product NDC
- 50090-5065
- 11-digit product format
- 500905065
- Labeler code
- 50090
- Product ID
- 50090-5065_e16fc423-653c-4607-95a5-8f482298c25b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- 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
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 |
|---|
| 50090-5065-0 | 50090506500 | 90 TABLET in 1 BOTTLE (50090-5065-0) | 90 tablet | 2020-05-29 | 0000-00-00 | No | No | Current |