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Methotrexate

NDC 0703-3678, Methotrexate, injection, solution, from Teva Parenteral Medicines, Inc..

Product NDC
0703-3678
Status
Listed
Labeler
Teva Parenteral Medicines, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRA-ARTERIAL, INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040843
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0703-3678 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • METHOTREXATE SODIUM25 mg/mL

Pharmacologic classes

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

Package NDCNDC-11Package
0703-3678-01007033678011 VIAL, SINGLE-DOSE in 1 CARTON (0703-3678-01) / 40 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/346ec9ce-dc98-4a55-b55e-d3af11f2d703

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0703-3678

Use it

Look up 0703-3678 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0703-3678 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0703-3678. 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.