DOFETILIDE
- Product NDC
- 50742-230
- 11-digit product format
- 507420230
- Labeler code
- 50742
- Product ID
- 50742-230_edc905ad-a1ad-4a93-8671-e4bade4abb24
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dofetilide
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Ingenus Pharmaceuticals, LLC
- Application
- ANDA212410
- Marketing category
- ANDA
- Marketing start
- 2020-01-07
- Marketing end
- 0000-00-00
- Substance
- DOFETILIDE
- Active strength
- 0 mg/1
- Pharmacologic classes
- Antiarrhythmic [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50742-230-60 | 50742023060 | 60 CAPSULE in 1 BOTTLE, PLASTIC (50742-230-60) | 60 capsule | 2020-01-07 | 0000-00-00 | No | No | Current |