Bumetanide
- Product NDC
- 71335-1246
- 11-digit product format
- 713351246
- Labeler code
- 71335
- Product ID
- 71335-1246_e4b2b9d3-bcce-4071-8703-2ed7341bc5f7
- 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
- 2 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71335-1246-1 | 71335124601 | 30 TABLET in 1 BOTTLE (71335-1246-1) | 30 tablet | 2017-10-18 | 0000-00-00 | No | No | Current |
| 71335-1246-2 | 71335124602 | 8 TABLET in 1 BOTTLE (71335-1246-2) | 8 tablet | 2017-10-18 | 0000-00-00 | No | No | Current |