# CARBOPLATIN

NDC: 55150-334
Generic name: CARBOPLATIN
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20160929

FDA application: ANDA205487

## Active ingredients

- CARBOPLATIN: 150 mg/15mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55150-334"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-334
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f5fe9a20-47a5-45b9-ab06-c6158d9b6aca