NDC 0185-0129
Bumetanide
Bumetanide
Bumetanide is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Eon Labs, Inc.. The primary component is Bumetanide.
| Product ID | 0185-0129_0541dab4-9ca2-4c8f-b70a-42f64547b808 |
| NDC | 0185-0129 |
| Product Type | Human Prescription Drug |
| Proprietary Name | Bumetanide |
| Generic Name | Bumetanide |
| Dosage Form | Tablet |
| Route of Administration | ORAL |
| Marketing Start Date | 1996-11-21 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA074700 |
| Labeler Name | Eon Labs, Inc. |
| Substance Name | BUMETANIDE |
| Active Ingredient Strength | 1 mg/1 |
| Pharm Classes | Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |