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Data / Drug companies / Metoprolol succinate er tablets

Metoprolol succinate er tablets: 8 companies and 35 products in the FDA NDC directory

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

Metoprolol succinate er tablets is listed in the FDA National Drug Code Directory by 8 companies, with 35 products in commercial distribution. 35 of the products (100.0%) are marketed under an abbreviated new drug application (ANDA), the generic route. The most common dosage forms are tablet, film coated, extended release, and the newest product started marketing on October 1, 2024.

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Companies listing it
8
Products
35
Generic (ANDA) products
35 (100.0%)
Application numbers
1
Routes
Oral
Brand names
Metoprolol Succinate
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Companies that list metoprolol succinate er tablets

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

CompanyProductsMain dosage formsMain marketing categoryNewest product started
Bryant Ranch Prepack11tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
A-S Medication Solutions5tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
Ascend Laboratories, LLC4tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
BluePoint Laboratories4tablet, film coated, extended releaseGeneric drugs (ANDA)May 14, 2021
Bryant Ranch Prepack4tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
Bryant Ranch Prepack3tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
Proficient Rx LP2tablet, film coated, extended releaseGeneric drugs (ANDA)November 27, 2020
Remedyrepack Inc.2tablet, film coated, extended releaseGeneric drugs (ANDA)October 1, 2024

Dosage forms

Dosage formProductsShare
Tablet, film coated, extended release35100%

Marketing categories

Marketing categoryProductsShare
Generic drugs (ANDA)35100%

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.