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Ondansetron EP Impurity A | CAS 153139-56-1 - Request Quote

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Ondansetron EP Impurity A

SZ CAT No:SZ-O002002
CAS No
153139-56-1
Mol.F.
C16H20N2O
Mol.Wt.
256.3
Inv. Status
In Stock
Rel. CAS No119812-29-2 (HCl salt)
Shipping Condition Room Temperature

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Usage Note:

Ondansetron EP Impurity A is chemically (3RS)-3-[(dimethylamino)methyl]-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one (as per EP & USP). It is also known as Ondansetron USP Related Compound A. Ondansetron EP Impurity A is supplied with detailed characterization data compliant with regulatory guideline. Ondansetron EP Impurity A can be used for the analytical method development, method validation (AMV), Quality Controlled (QC) application for Abbreviated New Drug Application (ANDA) or during commercial production of Ondansetron.

The product can be used as reference standards and further traceability against pharmacopeial standards (USP or EP) can be provided based on feasibility. SynZeal products are for analytical purpose only and not for human use.

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Ondansetron EP Impurity A for Method Validation

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Ondansetron EP Impurity A for ANDA Filing

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Ondansetron EP Impurity A Identification Standards

Ondansetron EP Impurity A for DMF Filing

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SynZeal will update these details as per new developments or findings in product specifications without further notice.

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