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icosapent ethyl

NDC 70710-1738, icosapent ethyl, capsule, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1738
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
CAPSULE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217656
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1738 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ICOSAPENT ETHYL.5 g/1
Package NDCNDC-11Package
70710-1738-470710173804240 CAPSULE in 1 BOTTLE (70710-1738-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5910742b-c5e6-4029-9a19-97669e3808bc

Use it

Look up 70710-1738 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1738 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1738. 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.