# Xatmep

NDC: 52652-2001
Generic name: Methotrexate
Labeler / Manufacturer: Azurity Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20170501

FDA application: NDA208400

## Active ingredients

- METHOTREXATE: 2.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52652-2001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52652-2001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aec9984e-34c5-481b-b6bf-9bb5caf1daf8