# Methotrexate Sodium

NDC: 64850-330
Generic name: Methotrexate Sodium
Labeler / Manufacturer: Elite Laboratories, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240516

FDA application: ANDA216453

## 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:"64850-330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64850-330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=89c05ea3-3be1-46dd-b112-29c436fd7289