Bumetanide
- Product NDC
- 50090-6304
- 11-digit product format
- 500906304
- Labeler code
- 50090
- Product ID
- 50090-6304_c3a19faf-7718-4b8c-b497-2e975a785ba8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- Substance
- BUMETANIDE
- Active strength
- 2 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 |
|---|
| 50090-6304-0 | 50090630400 | 90 TABLET in 1 BOTTLE (50090-6304-0) | 90 tablet | 2022-12-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Bumetanide Tablets, USP | A-S Medication Solutions | 2023-01-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |