FDA NDC Directory · JSON-LD · Markdown

CARBOPLATIN

NDC 69339-367 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerNatco Pharma USA LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077861
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsCARBOPLATIN (600 mg/60mL)
Marketing started20260702
Package count1

External sources

Source: openFDA. Public-domain (CC0).