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ot applicableNot applicableCanadaApo-valacyclovirTabletOralApotex Corporation2008-05-23Not applicableCanadaApo-valacyclovirTabletOralApotex Corporation2011-10-21Not applicableCanadaAuro-valacyclovirTabletOralAuro Pharma Inc2013-05-30Not applicableCanadaBio-valacyclovirTabletOralBiomed Pharma2016-04-07Not applicableCanadaDom-valacyclovirTabletOralDominion Pharmacal2010-07-01Not applicableCanadaJamp ValacyclovirTabletOralJamp Pharma CorporationNot applicableNot applicableCanadaJamp-valacyclovirTabletOralJamp Pharma Corporation2015-10-14Not applicableCanadaMar-valacyclovirTabletOralMarcan Pharmaceuticals Inc2015-10-202020-06-26CanadaMylan-valacyclovirTabletOralMylan Pharmaceuticals2010-05-25Not applicableCanada6-oxopurine / Alpha-amino acid ester / Amine / Aminopyrimidine / Aromatic heteropolycyclic compound / Azacycle / Azole / Carbonyl valacyclovir dosage for herpes simplex / Carboxylic acid ester / Fatty acid ester / Fatty acyl / Heteroaromatic compound / Hydrocarbon derivative / Hypoxanthine / Imidazole / Imidazopyrimidine / Monocarboxylic acid or derivatives / N-substituted imidazole / Organic nitrogen compound / Organic oxide / Organic oxygen compound / Organoheterocyclic compound / Organonitrogen compound / Organooxygen compound / Organopnictogen compound / Primary aliphatic amine / Primary amine / Purine / Pyrimidine / Pyrimidone / Valine or derivatives / Vinylogous amideBeutner KR: Valacyclovir: a review of its antiviral activity, pharmacokinetic properties, and clinical efficacy.

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    Continue to add approximately 5 mL aliquots of SSV to the mortar, mixing thoroughly between additions, until a concentrated suspension is produced, to a minimum total quantity of 20 mL SSV and a maximum total quantity of 40 mL SSV for both the 25 mg/mL and 50 mg/mL valacyclovir 1 mg dosages. Transfer the cherry flavor* to the mortar and dissolve in approximately 5 mL of SSV.

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    Data sources include IBM Watson Micromedex updated 10 Aug 2020 Cerner Multum updated 3 Aug 2020 Wolters Kluwer updated 10 Aug 2020 andothers.1993 The area under the drug concentration time curve approximates activity against VZV being about tenfold less.

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