bumetanide
- Product NDC
- 14539-701
- 11-digit product format
- 145390701
- Labeler code
- 14539
- Product ID
- 14539-701_138f8bdd-34a5-49c6-832f-0d343aa95c7b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Application
- ANDA074225
- Marketing category
- ANDA
- Marketing start
- 2019-06-01
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 14539-701-01 | 14539070101 | 100 TABLET in 1 BOTTLE (14539-701-01) | 100 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |
| 14539-701-05 | 14539070105 | 500 TABLET in 1 BOTTLE (14539-701-05) | 500 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |
| 14539-701-10 | 14539070110 | 1000 TABLET in 1 BOTTLE (14539-701-10) | 1000 tablet | 2019-06-01 | 0000-00-00 | No | No | Current |