# METHOTREXATE

NDC: 62332-730
Generic name: METHOTREXATE
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240604

FDA application: ANDA217552

## 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:"62332-730"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-730
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04a95db9-a124-4b97-bd71-1c37a6b3b0c8