Details for New Drug Application (NDA): 202900
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NDA 202900 describes BUMETANIDE, which is a drug marketed by Aspiro, Gland, Hospira, Lupin Ltd, MSN, Qilu Pharm Hainan, Sagent, Teva Parenteral, West-ward Pharms Int, Amneal Pharms Co, Appco, Heritage Pharma, Jubilant Generics, Mankind Pharma, Rising, Rubicon Research, Sandoz, Taro, Upsher Smith Labs, and Zydus Pharms, and is included in twenty-one NDAs. It is available from thirty-four suppliers. Additional details are available on the BUMETANIDE profile page.
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.
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 202900
| Tradename: | BUMETANIDE |
| Applicant: | Zydus Pharms |
| Ingredient: | bumetanide |
| Patents: | 0 |
Pharmacology for NDA: 202900
| Physiological Effect | Increased Diuresis at Loop of Henle |
Medical Subject Heading (MeSH) Categories for 202900
Suppliers and Packaging for NDA: 202900
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| BUMETANIDE | bumetanide | TABLET;ORAL | 202900 | ANDA | A-S Medication Solutions | 50090-6138 | 50090-6138-2 | 90 TABLET in 1 BOTTLE (50090-6138-2) |
| BUMETANIDE | bumetanide | TABLET;ORAL | 202900 | ANDA | Zydus Pharmaceuticals (USA) Inc. | 68382-525 | 68382-525-01 | 100 TABLET in 1 BOTTLE (68382-525-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 0.5MG | ||||
| Approval Date: | Apr 30, 2018 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 1MG | ||||
| Approval Date: | Apr 30, 2018 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 2MG | ||||
| Approval Date: | Apr 30, 2018 | TE: | AB | RLD: | No | ||||
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