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NDC 68788-8069-06 metoprolol succinate 25 mg/1 Details

metoprolol succinate 25 mg/1

metoprolol succinate is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is METOPROLOL SUCCINATE.

MedlinePlus Drug Summary

Metoprolol is used alone or in combination with other medications to treat high blood pressure. It also is used to prevent angina (chest pain) and to improve survival after a heart attack. Metoprolol also is used in combination with other medications to treat heart failure. Metoprolol 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: 68788-8069-06
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Metoprolol

Product Information

NDC	68788-8069
Product ID	68788-8069_4104232b-6aaa-4cc4-ae87-567f5c63f1dc
Associated GPIs	33200030057510
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	metoprolol succinate
Proprietary Name Suffix	n/a
Non-Proprietary Name	metoprolol succinate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	METOPROLOL SUCCINATE
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA203894
Listing Certified Through	2024-12-31

Package

NDC 68788-8069-06 (68788806906)

Pricing Information	N/A
NDC Package Code	68788-8069-6
Billing NDC	68788806906
Package	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8069-6)
Marketing Start Date	2021-08-23
NDC Exclude Flag	N