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NDC 51991-0819-01

propranolol hydrochloride 120 mg/1 CAPSULE, EXTENDED RELEASE

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NDC
51991-0819-01
Generic Name
propranolol hydrochloride
Brand Name
propranolol hydrochloride
Strength
120 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Breckenridge Pharmaceutical, 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…

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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