# Oxaliplatin

NDC: 60505-6287
Generic name: oxaliplatin
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240423

FDA application: ANDA204368

## Active ingredients

- OXALIPLATIN: 5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-6287"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6287
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb180ec5-1f75-43c1-9f63-c0657af2ca5f