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Data / Drug companies / Loxapine

Loxapine: 8 companies and 25 products in the FDA NDC directory

Loxapine is listed in the FDA National Drug Code Directory by 8 companies, with 25 products in commercial distribution. 24 of the products (96.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule; aerosol, powder, and the newest product started marketing on July 6, 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
8
Products
25
Generic (ANDA) products
24 (96.0%)
Application numbers
7
Routes
Oral, Respiratory (inhalation)
Brand names
Adasuve
openFDA record search
api.fda.gov

Companies that list loxapine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Remedyrepack Inc.6capsuleGeneric drugs (ANDA)March 17, 2025
Actavis Pharma, Inc.4capsuleGeneric drugs (ANDA)June 15, 1988
Elite Laboratories, Inc.4capsuleGeneric drugs (ANDA)January 27, 2020
Lannett Company, Inc.4capsuleGeneric drugs (ANDA)September 26, 2011
Coupler LLC3capsuleGeneric drugs (ANDA)January 30, 2025
Chartwell RX, LLC2capsuleGeneric drugs (ANDA)September 26, 2011
Alexza Pharmaceuticals, Inc.1aerosol, powderNew drug applications (NDA)July 6, 2026
Proficient Rx LP1capsuleGeneric drugs (ANDA)September 26, 2011

Dosage forms

Dosage formProductsShare
Capsule2496%
Aerosol, powder14%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2496%
New drug applications (NDA)14%

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.