Bumetanide
- Product NDC
- 63629-7440
- 11-digit product format
- 636297440
- Labeler code
- 63629
- Product ID
- 63629-7440_929508b6-25d1-4e93-aa23-4cbf7cecaabb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- NDA018225
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2015-10-15
- 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
- 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 |
|---|
| 63629-7440-1 | 63629744001 | 30 TABLET in 1 BOTTLE (63629-7440-1) | 30 tablet | 2017-11-13 | 0000-00-00 | No | No | Current |
| 63629-7440-2 | 63629744002 | 8 TABLET in 1 BOTTLE (63629-7440-2) | 8 tablet | 2017-11-13 | 0000-00-00 | No | No | Current |