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Methotrexate

NDC 47335-235, Methotrexate Sodium, tablet, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-235
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201749
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-235 \
  -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
47335-235-8347335023583100 TABLET in 1 BOTTLE (47335-235-83)
47335-235-964733502359636 TABLET in 1 BOTTLE (47335-235-96)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f1260de-b60c-4f0e-8af6-0e957b0a281b

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=47335-235

  • NADAC price for package 47335023583

    GET /v1/drugs/nadac/47335023583

  • NADAC price for package 47335023596

    GET /v1/drugs/nadac/47335023596

Use it

Look up 47335-235 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-235. 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.