NDC 69097-409

Metoprolol Succinate 200 mg tablet, extended release

On the label: Cipla USA., Inc..

Where it's made

Surat, India · makes the active ingredient

Problems found, fixed voluntarily Last FDA inspection Sep 2, 2022. 5 inspections on record, 1 with serious problems.

Indore, India · makes it, tests it, packages it and labels it

Serious problems, FDA action Last FDA inspection Feb 17, 2023. 6 inspections on record, 1 with serious problems.

Rubi, Spain · makes the active ingredient

Problems found, fixed voluntarily Last FDA inspection Nov 10, 2023. 6 inspections on record.

Generic drug: Metoprolol: see every company that makes it
Form: tablet, extended release, oral
Strength: 200 mg
Approval: ANDA ANDA207465
On the market since: Mar 25, 2019
Package NDCs: 69097-409-02 69097-409-07 69097-409-15
Official label: DailyMed (National Library of Medicine), updated Apr 7, 2023

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