DOFETILIDE
- Product NDC
- 72603-132
- 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 |
|---|
| 72603-132-01 | 60 CAPSULE in 1 BOTTLE (72603-132-01) | 2023-02-07 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dofetilide Capsules | NorthStar RxLLC | Sun Pharmaceutical Industries Limited | 2023-11-06 | Human Prescription Drug Label | 2 |