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Data / Drug companies / Carboplatin

Carboplatin: 11 companies and 40 products in the FDA NDC directory

Carboplatin is listed in the FDA National Drug Code Directory by 11 companies, with 40 products in commercial distribution. 38 of the products (95.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection, and the newest product started marketing on July 2, 2026.

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Companies listing it
11
Products
40
Generic (ANDA) products
38 (95.0%)
Application numbers
9
Routes
Intravenous
Brand names
Kyxata
openFDA record search
api.fda.gov

Companies that list carboplatin

Ranked by number of products. Finished drugs in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Teva Parenteral Medicines, Inc.8injection, solutionGeneric drugs (ANDA)January 19, 2016
Eugia US LLC6injection, solutionGeneric drugs (ANDA)August 3, 2020
Hospira, Inc.5injection, solutionGeneric drugs (ANDA)May 23, 2022
Bpi Labs LLC4injection, solutionGeneric drugs (ANDA)July 31, 2023
Gland Pharma Limited4injection, solutionGeneric drugs (ANDA)February 20, 2017
Natco Pharma USA LLC4injection, solutionGeneric drugs (ANDA)July 2, 2026
Teyro Labs Private Limited4injection, solutionGeneric drugs (ANDA)August 24, 2023
Avyxa Pharma, LLC2injectionNew drug applications (NDA)September 10, 2025
Accord Healthcare Inc.1injectionGeneric drugs (ANDA)September 19, 2017
Apotex Corp.1injection, solutionGeneric drugs (ANDA)January 18, 2007
Fresenius Kabi USA, LLC1injection, solutionGeneric drugs (ANDA)December 11, 2009

Dosage forms

Dosage formProductsShare
Injection, solution3792.5%
Injection37.5%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3895%
New drug applications (NDA)25%

Pharmacologic classes

ClassProducts
Platinum-based Drug40

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.