DOFETILIDE .25 mg/1
DOFETILIDE · CAPSULE · Sun Pharmaceutical Industries, Inc.
No Recall History
Plain English
DOFETILIDE is a capsule containing dofetilide at .25 mg/1, taken oral. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- DOFETILIDE
- Generic Name
- DOFETILIDE
- NDC Code (Product)
47335-062- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- .25 mg/1
- Dosage Form
- CAPSULE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA210466
- Drug Class
- Antiarrhythmic [EPC]
- Marketing Start
- 10/11/2018
Recall History
No Recall HistoryFrequently Asked Questions
What is DOFETILIDE used for?
DOFETILIDE contains DOFETILIDE. It is a capsule taken oral. Consult your doctor for specific uses.
Is DOFETILIDE a controlled substance?
DOFETILIDE is not classified as a controlled substance by the DEA.
What is the generic name for DOFETILIDE?
The generic name for DOFETILIDE is DOFETILIDE. There are 11 other brand versions of DOFETILIDE.
What is the NDC code for DOFETILIDE .25 mg/1?
The NDC (National Drug Code) for DOFETILIDE .25 mg/1 is 47335-062, listed by Sun Pharmaceutical Industries, Inc..