Bumetanide
- Product NDC
- 72162-2633
- 11-digit product format
- 721622633
- Labeler code
- 72162
- Product ID
- 72162-2633_80d48f46-53e7-428b-b03c-e22b7e0305d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA215364
- Marketing category
- ANDA
- Marketing start
- 2022-08-06
- 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
- 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 | .25 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 0Y2S3XUQ5H |
| Rxcui | 1727569 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2633-2 | Bumetanide | 10 in 1 CARTON | INJECTION | 10 | | 100 |
| 72162-2633-4 | Bumetanide | 4 mL in 1 VIAL | INJECTION | 4 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2633-2 | 72162263302 | 10 VIAL in 1 CARTON (72162-2633-2) / 4 mL in 1 VIAL (72162-2633-4) | 10 vial | 2026-05-06 | No | No | Historical |
| 72162-2633-4 | 72162263304 | 4 mL in 1 VIAL | 4 ml | | | | Historical |