Pravastatin 20mg (NDC: 0093-7201)

Name:

Pravastatin 20mg

NDC:

0093-7201

Generic Name:

Pravastatin Sodium

Strength:

20mg

Form:

Tablet

Labeler:

Teva Pharmaceuticals USA, Inc.

Shape:

Round

Color:

Yellow

Imprint:

TEVA;7201

Medication Class:

Statin

Active Ingredient:

Pravastatin Sodium

Pregnancy Category:

Do not use (Category X)

Illustration:

Pill Illustration: Pravastatin 20mg (0093-7201)

About this medication

Pravastatin is the name of the medication. It comes in the form of a tablet, and should be taken by mouth. It belongs to a class of medications called Statin.

Why is this medication prescribed

Cholesterol is a waxy, fat-like substance that occurs naturally in all parts of the body. Your body needs some cholesterol to work properly. If you have too much cholesterol in your blood, it can stick to the walls of your arteries. It can narrow them or even block them. High cholesterol (also called hyperlipidemia) is a serious condition that can lead to heart disease, stroke, kidney failure, and other health problems.

How does it work

Pravastatin belongs to a group of medications called Statins. It works by slowing the production of cholesterol in the body. Together with diet, exercise, and weight-loss it can reduce your cholesterol and reduce the risk of heart attack and stroke.

How to use it

This medication comes as a tablet. You should put it in your mouth and swallow it with a glass of water.

What to do if you are pregnant

Don't take this medication if you are pregnant or plan to become pregnant. Tell you physician if you are pregnant. Studies showed that mothers using the medication during pregnancy may have babies with problems related to the medicine and there are no situations where the medication can help the mother or baby enough to make the risk of problems worth it. This medication should never be used by pregnant women.

More Information

Read more about Pravastatin 20mg on the FDA website.

Last Update: May 13th 2017
Data sources: Label (May 13th 2017), National Institutes of Health (June 8th 2015), FDA (May 31st 2015)

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