Bumetanide
- Product NDC
- 72572-040
- 11-digit product format
- 725720040
- Labeler code
- 72572
- Product ID
- 72572-040_fee7772b-da97-4671-a532-553d74a49d36
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Civica, Inc.
- Application
- ANDA079196
- Marketing category
- ANDA
- Marketing start
- 2022-03-07
- Substance
- BUMETANIDE
- Active strength
- .25 mg/mL
- 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 | .25 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0Y2S3XUQ5H |
| Rxcui | 282486, 1727569 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72572-040-01 | Bumetanide | 4 mL in 1 VIAL | INJECTION | 4 | | 3 |
| 72572-040-10 | Bumetanide | 10 in 1 CARTON | INJECTION | 10 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72572-040 | BUMETANIDE INJECTION [CIVICA, INC.] | 3 | Current NDC, Legacy NDC, 2 package rows | 20230408_308c690f-c2bd-4c32-8728-42ec95425f77.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 |
|---|
| 72572-040-01 | 72572004001 | 4 mL in 1 VIAL | 4 ml | | | | | Historical |
| 72572-040-10 | 72572004010 | 10 VIAL in 1 CARTON (72572-040-10) / 4 mL in 1 VIAL (72572-040-01) | 10 vial | 2022-03-07 | 0000-00-00 | No | No | Current |