# Pemetrexed

NDC: 70069-834
Generic name: Pemetrexed disodium
Labeler / Manufacturer: Somerset Therapeutics LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250415

FDA application: ANDA211899

## Active ingredients

- PEMETREXED DISODIUM HEPTAHYDRATE: 100 mg/4mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-834"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-834
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=39219e4b-80a6-4d4f-96a3-1202e542d050