Bumetanide
- Product NDC
- 71335-1201
- 11-digit product format
- 713351201
- Labeler code
- 71335
- Product ID
- 71335-1201_33566b78-b939-4cd1-a3ef-1a297f8d2b84
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA209724
- Marketing category
- ANDA
- Marketing start
- 2017-10-18
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-1201-1 | 71335120101 | 30 TABLET in 1 BOTTLE (71335-1201-1) | 30 tablet | 2019-04-24 | 0000-00-00 | No | No | Current |
| 71335-1201-2 | 71335120102 | 90 TABLET in 1 BOTTLE (71335-1201-2) | 90 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1201-3 | 71335120103 | 28 TABLET in 1 BOTTLE (71335-1201-3) | 28 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1201-4 | 71335120104 | 18 TABLET in 1 BOTTLE (71335-1201-4) | 18 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |
| 71335-1201-5 | 71335120105 | 60 TABLET in 1 BOTTLE (71335-1201-5) | 60 tablet | 2021-12-28 | 0000-00-00 | No | No | Current |