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Data / Drug companies / Granisetron hydrochloride

Granisetron hydrochloride: 8 companies and 12 products in the FDA NDC directory

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Granisetron hydrochloride is listed in the FDA National Drug Code Directory by 8 companies, with 12 products in commercial distribution. 12 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are injection, solution; injection; tablet, film coated, and the newest product started marketing on July 4, 2025.

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Companies listing it
8
Products
12
Generic (ANDA) products
12 (100.0%)
Application numbers
8
Routes
Intravenous, Oral
Brand names
Granisol, Granisetron
openFDA record search
api.fda.gov

Companies that list granisetron hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Mylan Institutional LLC3injection, solutionGeneric drugs (ANDA)March 21, 2018
Eugia US LLC2injection, solutionGeneric drugs (ANDA)July 6, 2016
Hikma Pharmaceuticals USA Inc.2injectionGeneric drugs (ANDA)December 23, 2009
Bionpharma Inc.1tablet, film coatedGeneric drugs (ANDA)February 28, 2022
Breckenridge Pharmaceutical, Inc.1tabletGeneric drugs (ANDA)June 22, 2009
Fresenius Kabi USA, LLC1injection, solutionGeneric drugs (ANDA)November 20, 2009
Intra-Sana Laboratories1solutionGeneric drugs (ANDA)July 4, 2025
Natco Pharma Limited1tablet, film coatedGeneric drugs (ANDA)June 22, 2009

Dosage forms

Dosage formProductsShare
Injection, solution650%
Injection216.7%
Tablet, film coated216.7%
Solution18.3%
Tablet18.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)12100%

Pharmacologic classes

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.