Bumetanide
- Product NDC
- 50436-0129
- 11-digit product format
- 504360129
- Labeler code
- 50436
- Product ID
- 50436-0129_5e9a2c63-26ab-4ad8-a4ae-c0e683ad2843
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Unit Dose Services
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 50436-0129-1 | Bumetanide | 50 in 1 BOX, UNIT-DOSE | TABLET | 50 | | 2 |
| 50436-0129-1 | Bumetanide | 1 in 1 POUCH | TABLET | 1 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50436-0129 | BUMETANIDE TABLET [UNIT DOSE SERVICES] | 2 | Legacy NDC, 2 package rows | 20180403_805a6574-ce08-4dbd-a0f2-c423e14bb897.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 50436-0129-1 | 50436012901 | 50 in 1 BOX, UNIT-DOSE | Historical |