Skip to the page

Data / Drug companies / Cefprozil

Cefprozil: 7 companies and 23 products in the FDA NDC directory

Cefprozil is listed in the FDA National Drug Code Directory by 7 companies, with 23 products in commercial distribution. 23 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; powder, for suspension; tablet, and the newest product started marketing on May 4, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Companies listing it
7
Products
23
Generic (ANDA) products
23 (100.0%)
Application numbers
6
Routes
Oral
openFDA record search
api.fda.gov

Companies that list cefprozil

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Lupin Pharmaceuticals, Inc.5powder, for suspension; tabletGeneric drugs (ANDA)May 4, 2026
Aurobindo Pharma Limited4powder, for suspension; tablet, film coatedGeneric drugs (ANDA)May 24, 2007
NorthStar Rx LLC4powder, for suspension; tablet, film coatedGeneric drugs (ANDA)May 24, 2007
Rising Pharma Holdings, Inc.4tablet, film coated; powder, for suspensionGeneric drugs (ANDA)May 24, 2007
A-S Medication Solutions2tablet, film coated; powder, for suspensionGeneric drugs (ANDA)May 24, 2007
Ascend Laboratories, LLC2tablet, film coatedGeneric drugs (ANDA)January 20, 2025
Teva Pharmaceuticals USA, Inc.2tablet, film coatedGeneric drugs (ANDA)December 23, 2005

Dosage forms

Dosage formProductsShare
Tablet, film coated1147.8%
Powder, for suspension1043.5%
Tablet28.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)23100%

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.