# PEMRYDI RTU

NDC: 70121-2461
Generic name: Pemetrexed disodium
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20230606

FDA application: NDA215179

## Active ingredients

- PEMETREXED DISODIUM HEMIPENTAHYDRATE: 500 mg/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70121-2461"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70121-2461
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f006b06-ab85-423d-ba0c-dfc3fc25844e