Details for New Drug Application (NDA): 214474
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The generic ingredient in DEFERASIROX is deferasirox. There are twenty drug master file entries for this compound. Twenty-one suppliers are listed for this compound. Additional details are available on the deferasirox profile page.
Summary for 214474
Tradename: | DEFERASIROX |
Applicant: | Aurobindo Pharma Ltd |
Ingredient: | deferasirox |
Patents: | 0 |
Suppliers and Packaging for NDA: 214474
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DEFERASIROX | deferasirox | TABLET;ORAL | 214474 | ANDA | Aurobindo Pharma Limited | 59651-410 | 59651-410-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-410-30) |
DEFERASIROX | deferasirox | TABLET;ORAL | 214474 | ANDA | Aurobindo Pharma Limited | 59651-411 | 59651-411-30 | 30 TABLET, FILM COATED in 1 BOTTLE (59651-411-30) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 90MG | ||||
Approval Date: | Oct 16, 2023 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 180MG | ||||
Approval Date: | Oct 16, 2023 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 360MG | ||||
Approval Date: | Oct 16, 2023 | TE: | AB | RLD: | No |
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