DOFETILIDE
NDC 47335-063, DOFETILIDE, capsule, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-063
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA210466
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-063 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DOFETILIDE.5 mg/1
Pharmacologic classes
Antiarrhythmic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-063-79 | 47335006379 | 4 BLISTER PACK in 1 CARTON (47335-063-79) / 10 CAPSULE in 1 BLISTER PACK (47335-063-66) |
| 47335-063-86 | 47335006386 | 60 CAPSULE in 1 BOTTLE (47335-063-86) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e6caaf44-4a3e-46ef-85fa-f97f682fbdd6
Use it
Look up 47335-063 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-063 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-063. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.