Details for New Drug Application (NDA): 218746
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The generic ingredient in BUMETANIDE is bumetanide. There are six drug master file entries for this compound. Thirty-nine suppliers are listed for this compound. Additional details are available on the bumetanide profile page.
Summary for 218746
| Tradename: | BUMETANIDE |
| Applicant: | Aspiro |
| Ingredient: | bumetanide |
| Patents: | 0 |
Pharmacology for NDA: 218746
| Physiological Effect | Increased Diuresis at Loop of Henle |
Medical Subject Heading (MeSH) Categories for 218746
Suppliers and Packaging for NDA: 218746
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| BUMETANIDE | bumetanide | INJECTABLE;INJECTION | 218746 | ANDA | Camber Pharmaceuticals, Inc. | 31722-368 | 31722-368-32 | 10 VIAL, SINGLE-DOSE in 1 CARTON (31722-368-32) / 4 mL in 1 VIAL, SINGLE-DOSE (31722-368-31) |
| BUMETANIDE | bumetanide | INJECTABLE;INJECTION | 218746 | ANDA | Camber Pharmaceuticals, Inc. | 31722-369 | 31722-369-32 | 10 VIAL, MULTI-DOSE in 1 CARTON (31722-369-32) / 10 mL in 1 VIAL, MULTI-DOSE (31722-369-10) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | INJECTABLE;INJECTION | Strength | 0.25MG/ML | ||||
| Approval Date: | Feb 27, 2025 | TE: | AP | RLD: | No | ||||
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