# Methotrexate

NDC: 0703-3671
Generic name: Methotrexate
Labeler / Manufacturer: Teva Parenteral Medicines, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRA-ARTERIAL, INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS
Marketing started: 20120731

FDA application: ANDA040843

## Active ingredients

- METHOTREXATE SODIUM: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0703-3671"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0703-3671
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=346ec9ce-dc98-4a55-b55e-d3af11f2d703