# Methotrexate

NDC: 0143-9830
Generic name: Methotrexate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRA-ARTERIAL, INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS
Marketing started: 20050906

FDA application: ANDA040632

## Active ingredients

- METHOTREXATE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9830"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9830
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b080eb92-fc72-4ce6-a7ab-3f9ce2415526