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DOFETILIDE

NDC 47335-062, DOFETILIDE, capsule, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-062
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
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-062 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOFETILIDE.25 mg/1

Pharmacologic classes

Antiarrhythmic [EPC]

Package NDCNDC-11Package
47335-062-79473350062794 BLISTER PACK in 1 CARTON (47335-062-79) / 10 CAPSULE in 1 BLISTER PACK (47335-062-66)
47335-062-864733500628660 CAPSULE in 1 BOTTLE (47335-062-86)

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 47335-062 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-062 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-062. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.