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NDC 69238-2077-01

Propranolol Hydrochloride 10MG TABLET

In Stock at Premier Pharma
NDC
69238-2077-01
Generic Name
Propranolol Hydrochloride
Brand Name
Propranolol Hydrochloride
Strength
10MG
Dosage Form
TABLET
Route
ORAL
Package Size
—
Labeler
Amneal Pharmaceuticals NY LLC

FDA Drug Information

Indications & Usage

INDICATIONS AND USAGE Hypertension Propranolol hydrochloride tablets are indicated in the management of hypertension. It may be used alone or used in combination with other antihypertensive agents, particularly a thiazide diuretic. Propranolol hydrochloride is not indicated in the management of hypertensive emergencies. Angina Pectoris Due to Coronary Atherosclerosis Propranolol hydrochloride tablets are indicated to decrease angina frequency and increase exercise tolerance in patients with angi…

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

69238-2079-0140MGTABLET
In Stock
51991-0817-0160 mg/1CAPSULE, EXTENDED RELEASE
In Stock
69292-0530-0110 mg/1TABLET
2-Day
69292-0530-1010 mg/1TABLET
2-Day
51991-0819-01120 mg/1CAPSULE, EXTENDED RELEASE
2-Day

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