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Pralatrexate

NDC 65219-550, Pralatrexate, injection, from Fresenius Kabi USA, LLC.

Product NDC
65219-550
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA022468
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65219-550 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRALATREXATE20 mg/mL

Pharmacologic classes

Folate Analog Metabolic Inhibitor [EPC]

Package NDCNDC-11Package
65219-550-01652190550011 VIAL, SINGLE-DOSE in 1 CARTON (65219-550-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a5daa583-4965-4564-ad87-41ffe6c08a11

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=65219-550

Use it

Look up 65219-550 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-550 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-550. 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.