DOFETILIDE
- Product NDC
- 47335-063
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOFETILIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA210466
- Marketing category
- ANDA
- Substance
- DOFETILIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-063-79 | 4 BLISTER PACK in 1 CARTON (47335-063-79) / 10 CAPSULE in 1 BLISTER PACK (47335-063-66) | 20181011 | | No | Historical |
| 47335-063-86 | 60 CAPSULE in 1 BOTTLE (47335-063-86) | 20181011 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| e6caaf44-4a3e-46ef-85fa-f97f682fbdd6 | Dofetilide Capsules | Sun Pharmaceutical Industries, Inc. | Sun Pharmaceutical Industries Limited | 2023-11-01 | Human Prescription Drug Label | 7 |