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NDC 71335-1410-05 Labetalol HCL 300 mg/1 Details

Labetalol HCL 300 mg/1

Labetalol HCL is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is LABETALOL HYDROCHLORIDE.

MedlinePlus Drug Summary

Labetalol is used to treat high blood pressure. Labetalol 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: 71335-1410-05
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Labetalol

Product Information

NDC	71335-1410
Product ID	71335-1410_81a66469-1c03-486a-bf52-9489a866e866
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	Labetalol HCL
Proprietary Name Suffix	n/a
Non-Proprietary Name	Labetalol Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	300
Active Ingredient Units	mg/1
Substance Name	LABETALOL HYDROCHLORIDE
Labeler Name	Bryant Ranch Prepack
Pharmaceutical Class	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA200908
Listing Certified Through	2024-12-31

Package

NDC 71335-1410-05 (71335141005)

Pricing Information	N/A
NDC Package Code	71335-1410-5
Billing NDC	71335141005
Package	180 TABLET, FILM COATED in 1 BOTTLE (71335-1410-5)
Marketing Start Date	2019-12-03
NDC Exclude Flag	N