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Kineret

NDC 66658-234, anakinra, injection, solution, from Swedish Orphan Biovitrum AB (publ).

Product NDC
66658-234
Status
Listed
Labeler
Swedish Orphan Biovitrum AB (publ)
Dosage form
INJECTION, SOLUTION
Route
SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA103950
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66658-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ANAKINRA100 mg/.67mL

Pharmacologic classes

Interleukin 1 Receptor Antagonists [MoA]; Interleukin-1 Receptor Antagonist [EPC]

Package NDCNDC-11Package
66658-234-07666580234077 SYRINGE, GLASS in 1 CARTON (66658-234-07) / .67 mL in 1 SYRINGE, GLASS
66658-234-28666580234284 CARTON in 1 CASE (66658-234-28) / 7 SYRINGE, GLASS in 1 CARTON / .67 mL in 1 SYRINGE, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d9d74915-6606-4570-9c52-c4001d3177de

Use it

Look up 66658-234 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66658-234 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66658-234. 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.