Details for New Drug Application (NDA): 210466
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The generic ingredient in DOFETILIDE is dofetilide. There are thirteen drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the dofetilide profile page.
Summary for 210466
Tradename: | DOFETILIDE |
Applicant: | Sun Pharm |
Ingredient: | dofetilide |
Patents: | 0 |
Suppliers and Packaging for NDA: 210466
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DOFETILIDE | dofetilide | CAPSULE;ORAL | 210466 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-061 | 47335-061-79 | 4 BLISTER PACK in 1 CARTON (47335-061-79) / 10 CAPSULE in 1 BLISTER PACK (47335-061-66) |
DOFETILIDE | dofetilide | CAPSULE;ORAL | 210466 | ANDA | Sun Pharmaceutical Industries, Inc. | 47335-061 | 47335-061-86 | 60 CAPSULE in 1 BOTTLE (47335-061-86) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 0.125MG | ||||
Approval Date: | Oct 9, 2018 | TE: | AB | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 0.25MG | ||||
Approval Date: | Oct 9, 2018 | TE: | AB | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE;ORAL | Strength | 0.5MG | ||||
Approval Date: | Oct 9, 2018 | TE: | AB | RLD: | No |
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