Bumetanide
- Product NDC
- 70756-081
- 11-digit product format
- 707560081
- Labeler code
- 70756
- Product ID
- 70756-081_f131948c-e75a-4379-b9ec-875fea59a5fe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lifestar Pharma LLC
- Application
- ANDA219291
- Marketing category
- ANDA
- Marketing start
- 2025-04-03
- Substance
- BUMETANIDE
- Active strength
- 2 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 | 2 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 |
|---|
| 70756-081-11 | Bumetanide | 100 in 1 BOTTLE | TABLET | 100 | | 3 |
| 70756-081-51 | Bumetanide | 500 in 1 BOTTLE | TABLET | 500 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70756-081 | BUMETANIDE TABLET [LIFESTAR PHARMA LLC] | 3 | Current NDC, 2 package rows | 20250410_51a344b6-acf9-4ac4-b743-1e63e3df7958.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70756-081-11 | 70756008111 | 100 TABLET in 1 BOTTLE (70756-081-11) | 100 tablet | 2025-04-03 | No | No | Historical |
| 70756-081-51 | 70756008151 | 500 TABLET in 1 BOTTLE (70756-081-51) | 500 tablet | 2025-04-03 | No | No | Historical |