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Safety Data Sheet according to Regulation (EC) No. 1907/2006 (REACH) according to Regulation (EU) No. 2020/878 Trade name :110340 4Piperidone hydrochloride monohydrateRevision date : Print date :04/11/2022

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How to fill out dextromethorphan for system suitability

01

Weigh accurately about 100 mg of dextromethorphan hydrobromide reference standard into a 100 mL volumetric flask.

02

Dissolve the dextromethorphan hydrobromide reference standard in 70 mL of methanol, and sonicate for about 10 minutes to ensure complete dissolution.

03

Make up the volume to 100 mL with methanol, mix well and filter through a 0.45 μm membrane filter before use.

Who needs dextromethorphan for system suitability?

01

Pharmaceutical companies developing or testing drugs that contain dextromethorphan as an active ingredient may need dextromethorphan for system suitability.

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What is dextromethorphan for system suitability?

Dextromethorphan for system suitability refers to the use of this medication as a benchmark or control in a testing system to ensure accuracy, precision, and reliability in measurements during various analytical processes.

Who is required to file dextromethorphan for system suitability?

Manufacturers, researchers, and laboratories involved in the testing and analysis of pharmaceuticals are required to file dextromethorphan for system suitability to ensure compliance with regulatory standards.

How to fill out dextromethorphan for system suitability?

To fill out dextromethorphan for system suitability, one must complete the designated forms with accurate data regarding the concentration, method of preparation, testing conditions, and results, ensuring all information meets regulatory requirements.

What is the purpose of dextromethorphan for system suitability?

The purpose of dextromethorphan for system suitability is to validate the performance of the analytical method being used, ensuring that it operates within specified parameters and produces accurate results.

What information must be reported on dextromethorphan for system suitability?

Information that must be reported includes the batch number, potency, method of analysis, results from system suitability tests, and any deviations from expected outcomes.

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