Bumetanide
- Product NDC
- 50090-6308
- 11-digit product format
- 500906308
- Labeler code
- 50090
- Product ID
- 50090-6308_ec738c22-9dd0-489d-af8b-1103d67d78eb
- 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
- .5 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bumetanide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUMETANIDE | .5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0Y2S3XUQ5H |
| Rxcui | 197417 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6308-0 | Bumetanide | 90 in 1 BOTTLE | TABLET | 90 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6308 | BUMETANIDE TABLET [A-S MEDICATION SOLUTIONS] | 1 | Current NDC, Legacy NDC, 1 package rows | 20230106_f6ff0d37-c67d-4b9f-8b62-5deda9783c28.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-6308-0 | 50090630800 | 90 TABLET in 1 BOTTLE (50090-6308-0) | 90 tablet | 2022-12-30 | 0000-00-00 | No | No | Current |