Bumetanide
- Product NDC
- 71335-2705
- 11-digit product format
- 713352705
- Labeler code
- 71335
- Product ID
- 71335-2705_f8017e03-3d8c-4f73-ab38-a81008c7088a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074700
- Marketing category
- ANDA
- Marketing start
- 1996-11-21
- 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 | 197419 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2705-1 | Bumetanide | 30 in 1 BOTTLE | TABLET | 30 | | 100 |
| 71335-2705-2 | Bumetanide | 8 in 1 BOTTLE | TABLET | 8 | | 100 |
| 71335-2705-3 | Bumetanide | 100 in 1 BOTTLE | TABLET | 100 | | 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 |
|---|
| 71335-2705-1 | 71335270501 | 30 TABLET in 1 BOTTLE (71335-2705-1) | 30 tablet | 2025-07-28 | No | No | Historical |
| 71335-2705-2 | 71335270502 | 8 TABLET in 1 BOTTLE (71335-2705-2) | 8 tablet | 2025-07-28 | No | No | Historical |
| 71335-2705-3 | 71335270503 | 100 TABLET in 1 BOTTLE (71335-2705-3) | 100 tablet | 2025-07-28 | No | No | Historical |