Citalopram - NDSRI's


Frequently Asked Questions

Regulatory requirements for impurities in Citalopram are described in various pharmacopeias and regulatory guidelines such as ICH and USP.

The types of impurities in Citalopram include related substances, residual solvents, and inorganic impurities.

Acetonitrile or Methanol are the solvents used in analyzing many impurities in Citalopram.

Citalopram impurities are stored at a controlled room temperature between 2-8 °C or as indicated on the Certificate of Analysis (CoA).

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