# Pemfexy

NDC: 71390-250
Generic name: pemetrexed
Labeler / Manufacturer: Acacia Pharma, Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260622

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:"71390-250"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71390-250
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=caef07ce-066b-4c48-98dc-974b05ebbbe0