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Last Updated: November 16, 2024

Details for New Drug Application (NDA): 210466


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NDA 210466 describes DOFETILIDE, which is a drug marketed by Accord Hlthcare, Bionpharma, Dr Reddys Labs Sa, Granules, MSN, Novast Labs, Prinston Inc, Rk Pharma, Sigmapharm Labs Llc, Strides Pharma, Sun Pharm, and Teva Pharms Usa, and is included in twelve NDAs. It is available from sixteen suppliers. Additional details are available on the DOFETILIDE profile page.

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
Pharmacology for NDA: 210466
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:RXDosage:CAPSULE;ORALStrength0.125MG
Approval Date:Oct 9, 2018TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength0.25MG
Approval Date:Oct 9, 2018TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:CAPSULE;ORALStrength0.5MG
Approval Date:Oct 9, 2018TE:ABRLD:No

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