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NDC 51655-0281-25 Metoprolol Tartrate 50 mg/1 Details

Metoprolol Tartrate 50 mg/1

Metoprolol Tartrate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is METOPROLOL TARTRATE.

MedlinePlus Drug Summary

Metoprolol is used alone or in combination with other medications to treat high blood pressure. It also is used to treat chronic (long-term) angina (chest pain). Metoprolol is also used 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: 51655-0281-25
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Metoprolol

Product Information

NDC	51655-0281
Product ID	51655-281_e07d2b74-ae2c-cfeb-e053-2a95a90ae783
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	Metoprolol Tartrate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Metoprolol Tartrate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	50
Active Ingredient Units	mg/1
Substance Name	METOPROLOL TARTRATE
Labeler Name	Northwind Pharmaceuticals
Pharmaceutical Class	Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA200981
Listing Certified Through	2024-12-31

Package

NDC 51655-0281-25 (51655028125)

Pricing Information	N/A
NDC Package Code	51655-281-25
Billing NDC	51655028125
Package	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-281-25)
Marketing Start Date	2022-05-11
NDC Exclude Flag	N