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Methotrexate Sodium

NDC 64850-330, Methotrexate Sodium, tablet, from Elite Laboratories, Inc..

Product NDC
64850-330
Status
Listed
Labeler
Elite Laboratories, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216453
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64850-330 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHOTREXATE SODIUM2.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
64850-330-0164850033001100 TABLET in 1 BOTTLE, PLASTIC (64850-330-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/89c05ea3-3be1-46dd-b112-29c436fd7289
  • NADAC price for package 64850033001

    GET /v1/drugs/nadac/64850033001

Use it

Look up 64850-330 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64850-330 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64850-330. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.