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Get the free Label. DURLAZA (aspirin) Extended Release 162.5 mg Capsules - accessdata fda

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375 Morgan Lane Suite 203 West Haven, CT 06516 Phone: (203) 9344275 Fax: (203) 9344324 File name: Drama 30 count Trade Bottle Label Date: 7/7/15, 7/27/15, 8/6/15, 9/10/15 Control Number: 19806, 19868,
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How to fill out label durlaza aspirin extended:

01
Carefully read the instructions provided on the label.
02
Take one durlaza aspirin extended tablet orally, with water or food, as directed by your healthcare professional.
03
Do not crush, break, or chew the tablet, as it is designed to release the medication slowly over time.
04
If you are unsure about the dosage or any other aspect of taking durlaza aspirin extended, consult your healthcare professional for guidance.
05
Remember to take the medication at the same time each day to maintain a consistent blood level.
06
If you miss a dose, take it as soon as you remember. However, if it is close to the time for your next dose, skip the missed dose and resume your usual dosing schedule.
07
Store the durlaza aspirin extended tablets in a cool, dry place away from direct sunlight.

Who needs label durlaza aspirin extended:

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Individuals with a history of, or at risk for, cardiovascular diseases, such as heart attacks or strokes, may require durlaza aspirin extended as part of their treatment plan.
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Patients who have been prescribed durlaza aspirin extended specifically by their healthcare professional.
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It is essential to consult with a healthcare professional to determine if durlaza aspirin extended is appropriate for your health condition and to receive guidance on its usage.
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Durlaza aspirin extended is a medication used to help prevent blood clots.
Manufacturers and distributors of durlaza aspirin extended are required to file the label.
The label for durlaza aspirin extended should be filled out with all relevant information about the medication, including dosage instructions and warnings.
The purpose of the label is to provide important information to consumers about the medication and how to use it safely.
The label must include information such as the active ingredients, dosage instructions, side effects, and contraindications.
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