Nystatin Vaginal Suppositories
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This article is compiled based on the United States Pharmacopeia (USP) – 2025 Edition
Issued and maintained by the United States Pharmacopeial Convention (USP)
Nystatin Vaginal Suppositories contain not less than 90.0 percent and not more than 130.0 percent of the labeled amount of USP Nystatin Units.
Packaging and storage-Preserve in tight, light-resistant containers, at controlled room temperature.
USP Reference standards 〈11〉-
USP Nystatin RS
Water Determination, Method I 〈921〉: not more than 1.5%.
Assay-Proceed with Vaginal Suppositories as directed in the Assay under Nystatin Tablets.
