# Pemetrexed

NDC: 0781-3519
Generic name: Pemetrexed disodium
Labeler / Manufacturer: Sandoz Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220608

FDA application: NDA214657

## 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:"0781-3519"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3519
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ac04ab7-7f8c-46ce-ab56-a7a08cd02ab3