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Data / Drug companies / Pilocarpine hydrochloride

Pilocarpine hydrochloride: 14 companies and 27 products in the FDA NDC directory

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

Pilocarpine hydrochloride is listed in the FDA National Drug Code Directory by 14 companies, with 27 products in commercial distribution. 18 of the products (66.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated; solution/ drops; solution, and the newest product started marketing on October 20, 2026.

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Companies listing it
14
Products
27
Generic (ANDA) products
18 (66.7%)
Application numbers
10
Routes
Oral, Ophthalmic
Brand names
Salagen, Qlosi
openFDA record search
api.fda.gov

Companies that list pilocarpine hydrochloride

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Amneal Pharmaceuticals NY LLC3solution/ drops; tablet, film coatedGeneric drugs (ANDA)September 1, 2025
Amneal Pharmaceuticals NY LLC3solution/ dropsGeneric drugs (ANDA)September 23, 2020
Leading Pharma, LLC3solution/ dropsGeneric drugs (ANDA)October 20, 2026
Sandoz Inc3solution/ dropsAuthorized generics (NDA)September 30, 2011
Actavis Pharma, Inc.2tablet, film coatedAuthorized generics (NDA)September 13, 2011
Advanz Pharma (US) Corp.2tablet, film coatedNew drug applications (NDA)September 1, 2019
Aurobindo Pharma Limited2tablet, film coatedGeneric drugs (ANDA)August 13, 2019
Bryant Ranch Prepack2tablet, film coatedGeneric drugs (ANDA)October 14, 2005
Lannett Company, Inc.2tablet, film coatedGeneric drugs (ANDA)October 14, 2005
American Health Packaging1tablet, film coatedAuthorized generics (NDA)September 25, 2015
Amici Pharma, Inc.1tablet, film coatedGeneric drugs (ANDA)July 26, 2022
AvPAK1tablet, film coatedGeneric drugs (ANDA)January 7, 2021
Bryant Ranch Prepack1tablet, film coatedGeneric drugs (ANDA)October 14, 2005
Orasis Pharmaceuticals, Inc.1solutionNew drug applications (NDA)October 15, 2024

Dosage forms

Dosage formProductsShare
Tablet, film coated1555.6%
Solution/ drops1140.7%
Solution13.7%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1866.7%
Authorized generics (NDA)622.2%
New drug applications (NDA)311.1%

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.