Bumetanide
- Product NDC
- 50090-5666
- 11-digit product format
- 500905666
- Labeler code
- 50090
- Product ID
- 50090-5666_b626e5ea-7a48-4525-b9a3-d7c0739639dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA209724
- Marketing category
- ANDA
- Marketing start
- 2017-10-18
- 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 |
|---|
| 50090-5666-0 | 50090566600 | 30 TABLET in 1 BOTTLE (50090-5666-0) | 30 tablet | 2021-09-15 | No | No | Historical |
| 50090-5666-2 | 50090566602 | 90 TABLET in 1 BOTTLE (50090-5666-2) | 90 tablet | 2021-09-15 | No | No | Historical |