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Trexall

NDC 51285-366, Methotrexate, tablet, film coated, from Teva Women's Health LLC.

Product NDC
51285-366
Status
Listed
Labeler
Teva Women's Health LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040385
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51285-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHOTREXATE SODIUM5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51285-366-015128503660130 TABLET, FILM COATED in 1 BOTTLE (51285-366-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e942f8db-510f-44d6-acb5-b822196f5e8c

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=51285-366

  • NADAC price for package 51285036601

    GET /v1/drugs/nadac/51285036601

Use it

Look up 51285-366 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51285-366 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51285-366. 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.