bumetanide
- Product NDC
- 72603-298
- 11-digit product format
- 726030298
- Labeler code
- 72603
- Product ID
- 72603-298_3aa9066b-354b-4f6b-87b9-2752a3a51f6b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NorthStar Rx, LLC
- Application
- ANDA074225
- Marketing category
- ANDA
- Marketing start
- 2025-09-01
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- bumetanide
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BUMETANIDE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0Y2S3XUQ5H |
| Rxcui | 197417, 197418, 197419 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72603-298-01 | bumetanide | 100 in 1 BOTTLE | TABLET | 100 | | 1 |
| 72603-298-02 | bumetanide | 500 in 1 BOTTLE | TABLET | 500 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72603-298-01 | 72603029801 | 100 TABLET in 1 BOTTLE (72603-298-01) | 100 tablet | 2025-09-01 | No | No | Historical |
| 72603-298-02 | 72603029802 | 500 TABLET in 1 BOTTLE (72603-298-02) | 500 tablet | 2025-09-01 | No | No | Historical |