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Methotrexate

NDC 68071-3765, Methotrexate, tablet, from NuCare Pharmaceuticals, Inc..

Product NDC
68071-3765
Status
Listed
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210454
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3765 \
  -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
68071-3765-66807137650660 TABLET in 1 BOTTLE (68071-3765-6)
68071-3765-96807137650990 TABLET in 1 BOTTLE (68071-3765-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b61822e-b488-5eaf-e063-6394a90a2dcd

Use it

Look up 68071-3765 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-3765 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-3765. 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.