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What is Acyclovir Capsules USP Monograph about?

This document provides specifications for acyclovir capsules, including requirements for the active ingredient content, packaging and storage, identification, uniformity of dosage units, dissolution rate, limits on related compounds and residual solvents, and an assay method. Acyclovir capsules must contain between 93-107% of the labeled amount of acyclovir and meet tests for content uniformity, dissolution rate, and limits on impurities and residual solvents. The assay uses liquid chromatography with UV de

Author

ChengD

Language

EN