Bumetanide
- Product NDC
- 33261-983
- 11-digit product format
- 332610983
- Labeler code
- 33261
- Product ID
- 33261-983_ae72cf6a-bf5f-424c-8d8c-1aaffbb89826
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bumetanide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aidarex Pharmaceuticals LLC
- Application
- ANDA074225
- Marketing category
- ANDA
- Marketing start
- 2007-10-16
- Marketing end
- 0000-00-00
- Substance
- BUMETANIDE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Loop Diuretic [EPC],Increased Diuresis at Loop of Henle [PE]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 1d3f2f0a-cce7-32fe-77bf-6ee61839e736 | Product name | 9 | 20260113 |
| 601d9750-f415-d9d9-619c-0a87b4d3f237 | Product name | 3 | 20250331 |
| 594e2c86-3079-4e6e-96c9-48f7a8afc78d | Product name | 1 | 20230718 |
| 1d3f2f0a-cce7-32fe-77bf-6ee61839e736 | Product name | 2 | 20171211 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 33261-983-30 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ccee-f424-e053-dadaa90a57ce | BUMETANIDE TABLETS USP |
| 33261-983-90 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-ccee-f424-e053-dadaa90a57ce | BUMETANIDE TABLETS USP |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 33261-983-30 | Bumetanide | 30 in 1 BOTTLE, PLASTIC | TABLET | 30 | 1 | |
| 33261-983-90 | Bumetanide | 90 in 1 BOTTLE, PLASTIC | TABLET | 90 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 33261-983-30 | EA - Each | 33261-983 | 88c47aca-0d92-4d4e-80eb-1578fac687d5 | 1 | 2015-10-02 |
| 33261-983-90 | EA - Each | 33261-983 | 5fb8ad8c-a5ed-42e7-b7d4-4308e1d7874f | 1 | 2015-10-02 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| BUMETANIDE | ACTIVE INGREDIENT | 0Y2S3XUQ5H | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| BUMETANIDE | ACTIVE MOIETY | 0Y2S3XUQ5H | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| ALUMINUM OXIDE | INACTIVE INGREDIENT | LMI26O6933 | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| ANHYDROUS LACTOSE | INACTIVE INGREDIENT | 3SY5LH9PMK | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| D&C YELLOW NO. 10 | INACTIVE INGREDIENT | 35SW5USQ3G | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | BUMETANIDE TABLET [AIDAREX PHARMACEUTICALS LLC] | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 197418 | bumetanide 1 MG Oral Tablet | PSN | 1c4015ba-567a-403c-91f6-fad7749ea2a2 | 1 |
| 197418 | bumetanide 1 MG Oral Tablet | SCD | 1c4015ba-567a-403c-91f6-fad7749ea2a2 | 1 |
Packages#
| Package NDC | 11-digit format | Description | Status |
|---|---|---|---|
| 33261-983-30 | 33261098330 | 30 in 1 BOTTLE, PLASTIC | Historical |
| 33261-983-90 | 33261098390 | 90 in 1 BOTTLE, PLASTIC | Historical |