DOFETILIDE
- Product NDC
- 72603-131
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- DOFETILIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NorthStar RxLLC
- Application
- ANDA210466
- Marketing category
- ANDA
- Substance
- DOFETILIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 72603-131-01 | 60 CAPSULE in 1 BOTTLE (72603-131-01) | 20230207 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 4552d82a-dd28-410c-9642-1af060832b47 | Dofetilide Capsules | NorthStar RxLLC | Sun Pharmaceutical Industries Limited | 2023-11-06 | Human Prescription Drug Label | 2 |