# Methotrexate

NDC: 82804-136
Generic name: Methotrexate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200824

FDA application: ANDA213343

## Active ingredients

- METHOTREXATE SODIUM: 2.5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-136"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-136
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a76808f0-38a7-4b54-a4fb-3584f9058ae5