NDC 68382-565

metoprolol succinate 50 mg tablet, extended release

On the label: Zydus Pharmaceuticals (USA) Inc..

Where it's made

Zydus Lifesciences Limited

Ahmedabad, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Mar 24, 2023. 5 inspections on record.

Product details

Generic drug

Metoprolol: see every company that makes it

Form

tablet, extended release, oral

Strength

50 mg

Approval

ANDA ANDA203894

On the market since

Jun 7, 2018

Package NDCs

68382-565-01 68382-565-05 68382-565-10

Official label

DailyMed (National Library of Medicine), updated May 19, 2026

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