NDC 68382-0565-01
metoprolol succinate 50 mg/1 TABLET, EXTENDED RELEASE
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NDC
68382-0565-01
Generic Name
metoprolol succinate
Brand Name
metoprolol succinate
Strength
50 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Zydus Pharmaceuticals (USA) Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Metoprolol succinate extended-release tablets, are a beta-adrenergic blocker indicated for the treatment of: Hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. (1.1) Angina Pectoris. (1.2) Heart Failure, to reduce the risk of cardiovascular mortality and heart failure hospitalizations in patients with heart failure (1.3) 1.1 Hypertension Metoprolol succ…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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