Details for New Drug Application (NDA): 215137
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The generic ingredient in DEFERASIROX is deferasirox. There are twenty drug master file entries for this compound. Twenty-two suppliers are listed for this compound. Additional details are available on the deferasirox profile page.
Summary for 215137
| Tradename: | DEFERASIROX |
| Applicant: | Aurobindo Pharma |
| Ingredient: | deferasirox |
| Patents: | 0 |
Suppliers and Packaging for NDA: 215137
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DEFERASIROX | deferasirox | GRANULE;ORAL | 215137 | ANDA | Aurobindo Pharma Limited | 59651-447 | 59651-447-30 | 30 PACKET in 1 CARTON (59651-447-30) / 1 GRANULE in 1 PACKET (59651-447-38) |
| DEFERASIROX | deferasirox | GRANULE;ORAL | 215137 | ANDA | Aurobindo Pharma Limited | 59651-448 | 59651-448-30 | 30 PACKET in 1 CARTON (59651-448-30) / 1 GRANULE in 1 PACKET (59651-448-77) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | 90MG | ||||
| Approval Date: | Sep 8, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | 180MG | ||||
| Approval Date: | Sep 8, 2025 | TE: | AB | RLD: | No | ||||
Profile for product number 003
| Active Rx/OTC/Discontinued: | RX | Dosage: | GRANULE;ORAL | Strength | 360MG | ||||
| Approval Date: | Sep 8, 2025 | TE: | AB | RLD: | No | ||||
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