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NDC 68788-6855-03 Propranolol Hydrochloride 60 mg/1 Details

Propranolol Hydrochloride 60 mg/1

Propranolol Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is PROPRANOLOL HYDROCHLORIDE.

MedlinePlus Drug Summary

Propranolol is used to treat high blood pressure, irregular heart rhythms, pheochromocytoma (tumor on a small gland near the kidneys), certain types of tremor, and hypertrophic subaortic stenosis (a heart muscle disease). It is also used to prevent angina (chest pain), migraine headaches, and to improve survival after a heart attack. Propranolol is in a class of medications called beta blockers. It works by relaxing blood vessels and slowing heart rate to improve blood flow and decrease blood pressure. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Related Packages: 68788-6855-03
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Propranolol (Cardiovascular)

Product Information

NDC	68788-6855
Product ID	68788-6855_d2d138fd-64e6-4b5f-82c8-926508b7beb3
Associated GPIs	33100040107025
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Propranolol Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Propranolol Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	60
Active Ingredient Units	mg/1
Substance Name	PROPRANOLOL HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078494
Listing Certified Through	2024-12-31

Package

NDC 68788-6855-03 (68788685503)

Pricing Information	N/A
NDC Package Code	68788-6855-3
Billing NDC	68788685503
Package	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-6855-3)
Marketing Start Date	2016-12-13
NDC Exclude Flag	N