# Cisplatin

NDC: 44567-530
Generic name: cisplatin
Labeler / Manufacturer: WG Critical Care, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 20190405

FDA application: NDA018057

## Active ingredients

- CISPLATIN: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"44567-530"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=44567-530
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=508496cb-3441-46b3-a4fe-e0d440e6adc6