# Methotrexate

NDC: 0143-9516
Generic name: Methotrexate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRA-ARTERIAL, INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS
Marketing started: 20180105

FDA application: ANDA089343

## Active ingredients

- METHOTREXATE: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9516"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9516
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3989d30d-56e5-4e8d-9379-c30fecc894f2