# oxaliplatin

NDC: 42677-337
Generic name: oxaliplatin
Labeler / Manufacturer: Shandong New Time Pharmaceutical Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260115

FDA application: ANDA219765

## 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:"42677-337"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42677-337
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1ac38523-480b-4c0f-97a1-7dfa1432923c