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N-Nitroso Levofloxacin EP Impurity G (Possibility 2) - Request Quote

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N-Nitroso Levofloxacin EP Impurity G (Possibility 2)

SZ CAT No:SZ-L020034
CAS No
NA
Mol.F.
C16H17FN4O5
Mol.Wt.
364.3
Inv. Status
Under QC Approval

Chemical Name :

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Usage Note:

N-Nitroso Levofloxacin EP Impurity G (Possibility 2) is chemically (S)-9-Fluoro-3-methyl-10-((2-(methyl(nitroso)amino)ethyl)amino)-7-oxo-2,3-dihydro-7H-[1,4]oxazino[2,3,4-ij]quinoline-6-carboxylic acid. N-Nitroso Levofloxacin EP Impurity G (Possibility 2) is supplied with detailed characterization data compliant with regulatory guideline. N-Nitroso Levofloxacin EP Impurity G (Possibility 2) 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 Levofloxacin.

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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N-Nitroso Levofloxacin EP Impurity G (Possibility 2) for Method Validation

Levofloxacin Reference Standard

N-Nitroso Levofloxacin EP Impurity G (Possibility 2) for ANDA Filing

N-Nitroso Levofloxacin EP Impurity G (Possibility 2) for Forced Degradation Studies

N-Nitroso Levofloxacin EP Impurity G (Possibility 2) Identification Standards

N-Nitroso Levofloxacin EP Impurity G (Possibility 2) for DMF Filing

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SynZeal product information given on this website is as per the existing understanding while publishing the details on website. The customer is responsible for assessing the accuracy of the information at the time of actual purchase.

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

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