# PEMETREXED

NDC: 0409-2188
Generic name: PEMETREXED
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20220627

FDA application: NDA214218

## Active ingredients

- PEMETREXED DISODIUM: 500 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-2188"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-2188
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ae68628-7ab0-4491-b3ae-6a8330b719c8