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NDC 62559-0533-01

propranolol hydrochloride 160 mg/1 CAPSULE, EXTENDED RELEASE

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NDC
62559-0533-01
Generic Name
propranolol hydrochloride
Brand Name
Propranolol Hydrochloride ER
Strength
160 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
ANI Pharmaceuticals, Inc.

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Hypertension Propranolol hydrochloride extended-release capsules USP are indicated in the management of hypertension. They may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride extended-release capsules USP are not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride extended-release capsules USP are indicated to de…

Important Warnings

WARNINGS Angina Pectoris There have been reports of exacerbation of angina and, in some cases, myocardial infarction, following abrupt discontinuance of propranolol therapy. Therefore, when discontinuance of propranolol is planned, the dosage should be gradually reduced over at least a few weeks, and the patient should be cautioned against interruption or cessation of therapy without the physician…

Source: FDA. For professional use only. Not a substitute for prescribing information.

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