bumetanide
- Product NDC
- 50090-6138
- 11-digit product format
- 500906138
- Labeler code
- 50090
- Product ID
- 50090-6138_4529df9b-a34b-44ed-a1d1-03928d85db5e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202900
- Marketing category
- ANDA
- Marketing start
- 2018-05-01
- 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 |
|---|
| 50090-6138-2 | 50090613802 | 90 TABLET in 1 BOTTLE (50090-6138-2) | 90 tablet | 2022-10-03 | No | No | Historical |