# Pemetrexed

NDC: 72338-101
Generic name: Pemetrexed disodium
Labeler / Manufacturer: Waverley Pharma Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180604

FDA application: ANDA211899

## Active ingredients

- PEMETREXED DISODIUM HEPTAHYDRATE: 500 mg/20mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72338-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72338-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95633c32-89a8-4275-94e7-939c9f2e6135