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pemetrexed

NDC 70710-1655, pemetrexed disodium, injection, powder, lyophilized, for solution, from Zydus Pharmaceuticals USA Inc..

Product NDC
70710-1655
Status
Listed
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA214073
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1655 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PEMETREXED DISODIUM500 mg/20mL

Pharmacologic classes

Folate Analog Metabolic Inhibitor [EPC]; Folic Acid Metabolism Inhibitors [MoA]

Package NDCNDC-11Package
70710-1655-1707101655011 VIAL in 1 CARTON (70710-1655-1) / 20 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/363665ca-db15-4123-84ac-0ae66b5f1363

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70710-1655

Use it

Look up 70710-1655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70710-1655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70710-1655. 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.