Bumetanide
- Product NDC
- 72162-2632
- 11-digit product format
- 721622632
- Labeler code
- 72162
- Product ID
- 72162-2632_dd572e9b-8879-4f3a-9b7c-07901f6d8799
- 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 | 282486 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2632-2 | Bumetanide | 10 in 1 CARTON | INJECTION | 10 | | 100 |
| 72162-2632-4 | Bumetanide | 10 mL in 1 VIAL | INJECTION | 10 | | 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 |
|---|
| 72162-2632-2 | 72162263202 | 10 VIAL in 1 CARTON (72162-2632-2) / 10 mL in 1 VIAL (72162-2632-4) | 10 vial | 2026-05-06 | No | No | Historical |
| 72162-2632-4 | 72162263204 | 10 mL in 1 VIAL | 10 ml | | | | Historical |