NDC 47335-061-86

DOFETILIDE .125 mg/1

DOFETILIDE · CAPSULE

No Recall History

DOFETILIDE is a capsule containing dofetilide at a strength of .125 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..

Key Facts

Brand Name: DOFETILIDE
Generic Name: DOFETILIDE
NDC Code (Package): 47335-061-86
NDC Code (Product): 47335-061
Manufacturer: Sun Pharmaceutical Industries, Inc.
Strength: .125 mg/1
Dosage Form: CAPSULE
Route: ORAL
Marketing Status
Application #: ANDA210466
Drug Class: Antiarrhythmic [EPC]
Marketing Start: 10/11/2018

Recall History

No Recall History

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Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.