# CARBOPLATIN

NDC: 69339-366
Generic name: CARBOPLATIN
Labeler / Manufacturer: Natco Pharma USA LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260702

FDA application: ANDA077861

## Active ingredients

- CARBOPLATIN: 450 mg/45mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69339-366"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69339-366
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c89cedc-e48b-445c-ad05-54dbe60e4fb0