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All of our products require bacteriostatic water to reconstitute from solid to liquid form

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Food and Drug Administration Bacteriostatic Water for Injection USP labeling and 28-day in-use limit guidance

The first part of the study began by randomly dividing the test subjects in four groups including: wild type, APP/PS1, APP/PS1 + Dihexa administered at a dose of 1.44 mg/kg, and APP/PS1 + Dihexa administered at a dose of 2.88 mg/kg [1]