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Data / Drug companies / Amantadine

Amantadine: 10 companies and 14 products in the FDA NDC directory

Amantadine is listed in the FDA National Drug Code Directory by 10 companies, with 14 products in commercial distribution. 10 of the products (71.4%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet; capsule, coated pellets; capsule, and the newest product started marketing on January 19, 2026.

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Companies listing it
10
Products
14
Generic (ANDA) products
10 (71.4%)
Application numbers
4
Routes
Oral
Brand names
Gocovri
openFDA record search
api.fda.gov

Companies that list amantadine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Adamas Pharma, LLC2capsule, coated pelletsNew drug applications (NDA)August 24, 2017
Alembic Pharmaceuticals Inc.2tablet; capsuleGeneric drugs (ANDA)October 20, 2020
Alembic Pharmaceuticals Limited2capsule; tabletGeneric drugs (ANDA)October 20, 2020
Supernus Pharmaceuticals, Inc.2capsule, coated pelletsNew drug applications (NDA)August 24, 2017
American Health Packaging1capsuleGeneric drugs (ANDA)May 1, 2019
AvPAK1solutionGeneric drugs (ANDA)January 19, 2026
Coupler LLC1tabletGeneric drugs (ANDA)March 13, 2025
NCS HealthCare of Ky, LLC DBA Vangard Labs1tabletGeneric drugs (ANDA)October 20, 2020
Proficient Rx LP1tabletGeneric drugs (ANDA)October 20, 2020
Xttrium Laboratories, Inc.1solutionGeneric drugs (ANDA)November 5, 2024

Dosage forms

Dosage formProductsShare
Tablet535.7%
Capsule, coated pellets428.6%
Capsule321.4%
Solution214.3%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)1071.4%
New drug applications (NDA)428.6%

Pharmacologic classes

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.