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Data / Drug companies / Cyclosporine

Cyclosporine: 24 companies and 48 products in the FDA NDC directory

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

Cyclosporine is listed in the FDA National Drug Code Directory by 24 companies, with 48 products in commercial distribution. 32 of the products (66.7%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, liquid filled; emulsion; capsule, gelatin coated, and the newest product started marketing on September 21, 2026.

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Companies listing it
24
Products
48
Generic (ANDA) products
32 (66.7%)
Application numbers
22
Routes
Oral, Ophthalmic, Topical, Intravenous
Brand names
Neoral, Sandimmune, Gengraf, Cequa, Restasis, Verkazia, Restasis MultiDose
openFDA record search
api.fda.gov

Companies that list cyclosporine

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Apotex Corp.6capsule, liquid filled; capsule, gelatin coatedGeneric drugs (ANDA)February 7, 2022
Novartis Pharmaceuticals Corporation6capsule, liquid filled; injectionNew drug applications (NDA)July 14, 1995
Aurobindo Pharma Limited3capsule, liquid filledGeneric drugs (ANDA)September 17, 2026
Heritage Pharmaceuticals Inc. D/B/A Avet Pharmaceuticals Inc.3capsule, liquid filledGeneric drugs (ANDA)November 30, 2022
Strides Pharma Science Limited3capsule, liquid filledGeneric drugs (ANDA)August 16, 2022
Teva Pharmaceuticals USA, Inc.3capsule, liquid filledGeneric drugs (ANDA)June 8, 2021
AbbVie Inc.2capsuleGeneric drugs (ANDA)November 1, 2015
Allergan, Inc.2emulsionNew drug applications (NDA)November 10, 2016
American Health Packaging2capsule, gelatin coatedGeneric drugs (ANDA)November 3, 2015
Dr. Reddy's Laboratories Inc.2capsule, liquid filledGeneric drugs (ANDA)July 1, 2024
Qilu Pharmaceutical Co., Ltd.2capsule, liquid filledGeneric drugs (ANDA)September 15, 2025
Sun Pharmaceutical Industries, Inc.2solution/ dropsNew drug applications (NDA)August 15, 2018
A-S Medication Solutions1emulsionNew drug applications (NDA)April 1, 2003
Cipla USA Inc.1emulsionGeneric drugs (ANDA)September 21, 2026
Devatis, Inc.1emulsionGeneric drugs (ANDA)July 4, 2024
Harrow Eye, LLC1emulsionNew drug applications (NDA)February 1, 2022
KVK-Tech, Inc.1emulsionAuthorized generics (NDA)February 10, 2022
Lupin Pharmaceuticals, Inc.1emulsionAuthorized generics (NDA)May 11, 2022
Mylan Pharmaceuticals Inc.1emulsionGeneric drugs (ANDA)February 3, 2022
Santen Incorporated1emulsionNew drug applications (NDA)February 1, 2022
Saptalis Pharmaceuticals, LLC.1emulsionGeneric drugs (ANDA)December 12, 2025
Teva Pharmaceuticals USA, Inc.1solutionGeneric drugs (ANDA)March 29, 2005
Teva Pharmaceuticals, Inc.1emulsionGeneric drugs (ANDA)October 28, 2025
Upsher-Smith Laboratories, LLC1emulsionGeneric drugs (ANDA)March 27, 2026

Dosage forms

Dosage formProductsShare
Capsule, liquid filled2347.9%
Emulsion1429.2%
Capsule, gelatin coated48.3%
Capsule24.2%
Solution/ drops24.2%
Solution24.2%
Injection12.1%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)3266.7%
New drug applications (NDA)1327.1%
Authorized generics (NDA)36.2%

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.