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NDC 69292-0532-01

Propranolol Hydrochloride 20 mg/1 TABLET

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NDC
69292-0532-01
Generic Name
Propranolol Hydrochloride
Brand Name
Propranolol Hydrochloride
Strength
20 mg/1
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
AMICI PHARMACEUTICALS LLC

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Hypertension Propranolol hydrochloride tablets, 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 tablets, USP are not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride tablets, USP are indicated to decrease angina frequency and increase exercise toler…

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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Other Propranolol Hydrochloride NDC Codes

69238-2077-0110MGTABLET
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69238-2079-0140MGTABLET
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51991-0817-0160 mg/1CAPSULE, EXTENDED RELEASE
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69292-0530-0110 mg/1TABLET
2-Day
69292-0530-1010 mg/1TABLET
2-Day

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