# Carboplatin

NDC: 63323-172
Generic name: CARBOPLATIN
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20091211

FDA application: ANDA077266

## Active ingredients

- CARBOPLATIN: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-172"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-172
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b4fa7aac-c9d2-4af4-a281-3e6cfc502ff6