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Data / Drug companies / Omeprazole magnesium

Omeprazole magnesium: 21 companies and 27 products in the FDA NDC directory

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

Omeprazole magnesium is listed in the FDA National Drug Code Directory by 21 companies, with 27 products in commercial distribution. 23 of the products (85.2%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are capsule, delayed release; tablet, delayed release; granule, delayed release, and the newest product started marketing on September 1, 2026.

The request: Get every company that lists omeprazole magnesium in the FDA NDC directory, with headquarters, website and number of employees. $10 of work on sign-up, no card.

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Companies listing it
21
Products
27
Generic (ANDA) products
23 (85.2%)
Application numbers
6
Routes
Oral
Brand names
Prilosec Otc, Omeprazole, Omeprazole, Prilosec, Equate Omeprazole, Basic Care Omeprazole, Acid Reducer
openFDA record search
api.fda.gov

Companies that list omeprazole magnesium

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Walgreen Company3capsule, delayed releaseGeneric drugs (ANDA)April 9, 2024
Covis Pharma US, Inc2granule, delayed releaseNew drug applications (NDA)August 25, 2017
Safeway2capsule, delayed releaseGeneric drugs (ANDA)June 3, 2024
The Procter & Gamble Manufacturing Company2tablet, delayed releaseGeneric drugs (ANDA)September 1, 2025
The Procter & Gamble Manufacturing Company2tablet, delayed releaseNew drug applications (NDA)August 15, 2012
Amazon.com Services LLC1capsule, delayed releaseGeneric drugs (ANDA)February 22, 2023
CVS Pharmacy1capsule, delayed releaseGeneric drugs (ANDA)November 1, 2011
CVS Woonsocket Prescription Center, Incorporated1capsule, delayed releaseGeneric drugs (ANDA)April 1, 2025
Cardinal Health 110, LLC. DBA Leader1capsule, delayed releaseGeneric drugs (ANDA)March 7, 2017
Chain Drug Consortium, LLC1capsule, delayed releaseGeneric drugs (ANDA)January 1, 2016
Chain Drug Marketing Association1capsule, delayed releaseGeneric drugs (ANDA)January 1, 2016
Chain Drug Marketing Association, Inc.1capsule, delayed releaseGeneric drugs (ANDA)January 1, 2016
Discount Drug Mart1capsule, delayed releaseGeneric drugs (ANDA)November 18, 2016
Dr. Reddy's Laboratories Inc.1capsule, delayed releaseGeneric drugs (ANDA)December 26, 2018
Dr. Reddy's Laboratories Limited1capsule, delayed releaseGeneric drugs (ANDA)March 1, 2010
Geri-Care Pharmaceuticals, Corp1capsule, delayed releaseGeneric drugs (ANDA)April 1, 2013
H E B1capsule, delayed releaseGeneric drugs (ANDA)January 1, 2016
Meijer, Inc.1capsule, delayed releaseGeneric drugs (ANDA)August 24, 2023
Target Corporation1capsule, delayed releaseGeneric drugs (ANDA)July 21, 2018
Walmart Inc.1capsule, delayed releaseGeneric drugs (ANDA)November 30, 2022
Yyba Corp1capsule, delayed releaseGeneric drugs (ANDA)September 1, 2026

Dosage forms

Dosage formProductsShare
Capsule, delayed release2177.8%
Tablet, delayed release414.8%
Granule, delayed release27.4%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)2385.2%
New drug applications (NDA)414.8%

Pharmacologic classes

ClassProducts
Proton Pump Inhibitor27

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.