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Data / Drug companies / Capsule, delayed release pellets

Companies that list capsule, delayed release pellets products: 33 companies and 104 products in the FDA NDC directory

The FDA National Drug Code Directory lists 104 products that are capsule, delayed release pellets products from 33 companies. The ten largest listers hold 54.8% of them, and the newest started marketing on August 12, 2026.

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Companies
33
Products
104
Drugs by generic name
11
Main marketing category
Generic drugs (ANDA)

Companies that list capsule, delayed release pellets products

Ranked by number of products in commercial distribution.

CompanyProductsMain dosage formsMain marketing categoryNewest product started
AbbVie Inc.8capsule, delayed release pelletsBiologics (BLA)October 12, 2023
Actavis Pharma, Inc.6capsule, delayed release pelletsDrugs for further processingFebruary 1, 2024
Bryant Ranch Prepack6capsule, delayed release pelletsGeneric drugs (ANDA)May 21, 2018
Mylan Pharmaceuticals Inc.6capsule, delayed release pelletsGeneric drugs (ANDA)January 22, 2024
Towa Pharmaceutical Europe, S.L.6capsule, delayed release pelletsDrugs for further processingJune 1, 2018
Abbott Laboratories GmbH5capsule, delayed release pelletsExport onlyOctober 21, 2013
Aphena Pharma Solutions - Tennessee, LLC5capsule, delayed release pelletsGeneric drugs (ANDA)July 3, 2017
Breckenridge Pharmaceutical, Inc.5capsule, delayed release pelletsGeneric drugs (ANDA)March 27, 2023
Bryant Ranch Prepack5capsule, delayed release pelletsGeneric drugs (ANDA)May 21, 2018
Bryant Ranch Prepack5capsule, delayed release pelletsGeneric drugs (ANDA)September 1, 2017
Golden State Medical Supply, Inc.5capsule, delayed release pelletsGeneric drugs (ANDA)July 3, 2017
Preferred Pharmaceuticals Inc.5capsule, delayed release pelletsGeneric drugs (ANDA)August 12, 2026
Quallent Pharmaceuticals Health LLC4capsule, delayed release pelletsGeneric drugs (ANDA)May 21, 2018
A-S Medication Solutions3capsule, delayed release pelletsGeneric drugs (ANDA)November 1, 2021
Hawaii Repack, Inc.3capsule, delayed release pelletsGeneric drugs (ANDA)December 17, 2013
Proficient Rx LP3capsule, delayed release pelletsGeneric drugs (ANDA)June 11, 2014
Yaopharma Co., Ltd.3capsule, delayed release pelletsGeneric drugs (ANDA)January 1, 2024
Fournier Laboratories Ireland LTD2capsule, delayed release pelletsDrugs for further processingAugust 23, 2024
Horizon Therapeutics USA, Inc.2capsule, delayed release pelletsNew drug applications (NDA)April 30, 2013
Lannett Company, Inc.2capsule, delayed release pelletsGeneric drugs (ANDA)September 1, 2017
Mayne Pharma International Pty Ltd2capsule, delayed release pelletsDrugs for further processingMay 20, 2019
NuCare Pharmaceuticals,Inc.2capsule, delayed release pelletsGeneric drugs (ANDA)June 11, 2014
Advanced Rx of Tennessee, LLC1capsule, delayed release pelletsGeneric drugs (ANDA)December 17, 2013
Asclemed USA, Inc.1capsule, delayed release pelletsGeneric drugs (ANDA)December 17, 2013
BluePoint Laboratories1capsule, delayed release pelletsGeneric drugs (ANDA)May 21, 2018
Dr. Reddy's Laboratories Inc.1capsule, delayed release pelletsAuthorized generics (NDA)September 1, 2024
Dr. Reddy's Laboratories Limited1capsule, delayed release pelletsGeneric drugs (ANDA)March 24, 2010
Jaymac Pharmaceuticals, LLC1capsule, delayed release pelletsOther unapproved drugsAugust 12, 2011
Mylan Institutional Inc.1capsule, delayed release pelletsGeneric drugs (ANDA)December 1, 2009
Proficient Rx LP1capsule, delayed release pelletsGeneric drugs (ANDA)May 21, 2018
Proficient Rx LP1capsule, delayed release pelletsGeneric drugs (ANDA)December 17, 2013
Remedyrepack Inc.1capsule, delayed release pelletsGeneric drugs (ANDA)January 13, 2017
Safecor Health, LLC1capsule, delayed release pelletsGeneric drugs (ANDA)June 16, 2026

Drugs most often listed

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.