# Pemfexy

NDC: 42367-531
Generic name: pemetrexed
Labeler / Manufacturer: Eagle Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20220201
Marketing ended: 20280430
FDA application: NDA209472

## Active ingredients

- PEMETREXED MONOHYDRATE: 25 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42367-531"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42367-531
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2308f4e8-21c8-49c1-a5b8-deb8610bac6a