# Methotrexate

NDC: 61703-408
Generic name: Methotrexate
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, SUBCUTANEOUS
Marketing started: 20131111

FDA application: NDA011719

## 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:"61703-408"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61703-408
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e30eaef-5a09-4104-8a11-c32933eadeab