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NDC 51655-0302-26 Propranolol Hydrochloride 20 mg/1 Details

Propranolol Hydrochloride 20 mg/1

Propranolol Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is PROPRANOLOL HYDROCHLORIDE.

MedlinePlus Drug Summary

Propranolol is used alone or in combination with other medications to treat high blood pressure. It is also used to treat irregular heartbeats, pheochromocytoma (tumor on a small gland near the kidneys), certain types of tremor, and hypertrophic subaortic stenosis (a heart muscle disease). Propranolol 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: 51655-0302-26
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Propranolol (Cardiovascular)

Product Information

NDC	51655-0302
Product ID	51655-302_f2b8adcb-4d63-daa1-e053-2995a90ae4c4
Associated GPIs
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	TABLET
Route	ORAL
Active Ingredient Strength	20
Active Ingredient Units	mg/1
Substance Name	PROPRANOLOL HYDROCHLORIDE
Labeler Name	Northwind Pharmaceuticals, LLC
Pharmaceutical Class	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA070221
Listing Certified Through	2024-12-31

Package

NDC 51655-0302-26 (51655030226)

Pricing Information	N/A
NDC Package Code	51655-302-26
Billing NDC	51655030226
Package	90 TABLET in 1 BOTTLE, PLASTIC (51655-302-26)
Marketing Start Date	2020-05-19
NDC Exclude Flag	N