Bumetanide
- Product NDC
- 50090-5664
- 11-digit product format
- 500905664
- Labeler code
- 50090
- Product ID
- 50090-5664_1b3acb4a-bcb0-42d5-8600-6bf02fcc06c0
- 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
- .5 mg/1
- Pharmacologic classes
- Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bumetanide
- Listing expiration
- 2027-12-31
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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5664-0 | Bumetanide | 90 in 1 BOTTLE | TABLET | 90 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5664 | BUMETANIDE TABLET [A-S MEDICATION SOLUTIONS] | 6 | Current NDC, Legacy NDC, 1 package rows | 20231210_f4326e53-5217-48d4-a089-1184442049ac.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 |
|---|
| 50090-5664-0 | 50090566400 | 90 TABLET in 1 BOTTLE (50090-5664-0) | 90 tablet | 2021-09-15 | 0000-00-00 | No | No | Current |