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Data / Drug companies / Famotidine, calcium carbonate and magnesium hydroxide

Famotidine, calcium carbonate and magnesium hydroxide: 20 companies and 23 products in the FDA NDC directory

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

Famotidine, calcium carbonate and magnesium hydroxide is listed in the FDA National Drug Code Directory by 20 companies, with 23 products in commercial distribution. 23 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, chewable, and the newest product started marketing on July 16, 2026.

The request: Get every company that lists famotidine, calcium carbonate and magnesium hydroxide 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
20
Products
23
Generic (ANDA) products
23 (100.0%)
Application numbers
1
Routes
Oral
Brand names
Dual Action Complete, Basic Care Dual Action Complete, Signature Care Acid Reducer Complete, Equaline Complete Dual Action, DG Health Acid Reducer Complete, Up and Up Dual Action Acid Reducer Antacid, Acid Reducer Complete, Good Sense Dual Action Complete
openFDA record search
api.fda.gov

Companies that list famotidine, calcium carbonate and magnesium hydroxide

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Amazon.com Services LLC2tablet, chewableGeneric drugs (ANDA)July 16, 2026
L. Perrigo Company2tablet, chewableGeneric drugs (ANDA)August 9, 2022
Safeway2tablet, chewableGeneric drugs (ANDA)August 22, 2025
American Sales Company1tablet, chewableGeneric drugs (ANDA)September 29, 2016
Amerisource Bergen1tablet, chewableGeneric drugs (ANDA)March 10, 2026
CVS Pharmacy1tablet, chewableGeneric drugs (ANDA)February 11, 2016
CVS Woonsocket Prescription Center, Incorporated1tablet, chewableGeneric drugs (ANDA)July 13, 2026
Cardinal Health 110, LLC. DBA Leader1tablet, chewableGeneric drugs (ANDA)December 14, 2021
Dolgencorp, Inc. (dollar General & Rexall)1tablet, chewableGeneric drugs (ANDA)December 27, 2018
H E B1tablet, chewableGeneric drugs (ANDA)April 7, 2016
HyVee Inc1tablet, chewableGeneric drugs (ANDA)August 11, 2008
Kroger Company1tablet, chewableGeneric drugs (ANDA)February 1, 2016
Meijer Distribution Inc1tablet, chewableGeneric drugs (ANDA)January 26, 2016
Publix Super Markets Inc1tablet, chewableGeneric drugs (ANDA)November 6, 2018
Strategic Sourcing Services LLC1tablet, chewableGeneric drugs (ANDA)October 31, 2023
Target Corporation1tablet, chewableGeneric drugs (ANDA)January 8, 2025
Topco Associates LLC1tablet, chewableGeneric drugs (ANDA)February 29, 2016
United Natural Foods, Inc. DBA Unfi1tablet, chewableGeneric drugs (ANDA)September 2, 2008
Wal-Mart Stores Inc1tablet, chewableGeneric drugs (ANDA)August 8, 2008
Walgreen Company1tablet, chewableGeneric drugs (ANDA)January 29, 2016

Dosage forms

Dosage formProductsShare
Tablet, chewable23100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)23100%

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.