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the values above reflect the manufacturer's published product standard
You still react, or you simply do not want to manage the careful layering required to keep them working
Which category your vial falls into, and its exact window, comes from your prescription label and pharmacy
To report SUSPECTED ADVERSE EVENTS, contact Actavis at 1-800-272-5525 or FDA at 1-800-FDA-1088 or for voluntary reporting of adverse reactions
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