NDC 75907-346

Metoprolol succinate 200 mg tablet, film coated, extended release

On the label: Dr. Reddy's Laboratories Inc..

Where it's made

Dr. Reddy's Laboratories Limited

Medchal-Malkajgiri, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Oct 27, 2023. 8 inspections on record.

Product details

Generic drug
Metoprolol: see every company that makes it
Form
tablet, film coated, extended release, oral
Strength
200 mg
Approval
ANDA ANDA078889
On the market since
Jan 13, 2026
Package NDCs
75907-346-01 75907-346-05
Official label
DailyMed (National Library of Medicine), updated Jan 13, 2026

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