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SIMPONI ARIA

NDC 57894-350, golimumab, solution, from Janssen Biotech, Inc..

Product NDC
57894-350
Status
Listed
Labeler
Janssen Biotech, Inc.
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
BLA
Application
BLA125433
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57894-350 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GOLIMUMAB50 mg/4mL

Pharmacologic classes

Tumor Necrosis Factor Blocker [EPC]; Tumor Necrosis Factor Receptor Blocking Activity [MoA]

Package NDCNDC-11Package
57894-350-01578940350011 VIAL, SINGLE-DOSE in 1 CARTON (57894-350-01) / 4 mL in 1 VIAL, SINGLE-DOSE
57894-350-89578940350891 VIAL, SINGLE-DOSE in 1 CARTON (57894-350-89) / 4 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9e260a47-55af-4c92-8d88-a86ccc767fff

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=57894-350

Use it

Look up 57894-350 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57894-350 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57894-350. 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.