# pemetrexed

NDC: 70710-1674
Generic name: pemetrexed disodium
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220526

FDA application: ANDA214073

## Active ingredients

- PEMETREXED DISODIUM: 1000 mg/40mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1674"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1674
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=363665ca-db15-4123-84ac-0ae66b5f1363