Bumetanide
- Product NDC
- 82804-119
- 11-digit product format
- 828040119
- Labeler code
- 82804
- Product ID
- 82804-119_6e3d3ea1-830f-4fc6-9c56-b2ec71875dc6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 0Y2S3XUQ5H | BUMETANIDE | 28395-03-1 | BUMETANIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82804-119-90 | 82804011990 | 90 TABLET in 1 BOTTLE (82804-119-90) | 90 tablet | 2024-07-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bumetanide Tablets, USP | Proficient Rx LP | 2024-07-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |