# Cisplatin

NDC: 68001-283
Generic name: Cisplatin
Labeler / Manufacturer: BluePoint Laboratories
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20160802

FDA application: ANDA206774

## Active ingredients

- CISPLATIN: 1 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68001-283"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68001-283
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a60c5173-6bc0-4c9d-9674-b3f4d68f79ba