USPUSP-NF
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Olmesartan Medoxomil Compounded Oral Suspension

BRIEFING

Olmesartan Medoxomil Compounded Oral Suspension. Because there is no existing USP monograph for this compounded preparation, a new monograph based on a validated stability-indicating method for assessing stability is proposed. The liquid chromatographic procedure in the Assay is based on analyses validated using the XBridge brand of analytical column with L1 packing. The typical retention time for olmesartan medoxomil is about 5.7 min.

 Please submit comments to CompoundingSL@usp.org.

 (CMP: B. Groat)

 Case ID—SUB-1354

USP REFERENCE STANDARDS FOR PURCHASE

USP Olmesartan Medoxomil RS
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