At NINGBO INNO PHARMCHEM CO.,LTD., we understand that the integrity of pharmaceutical products hinges on precise quality control. Central to this is the use of pharmaceutical reference standards, and Ceftazidime Pentahydrate (CAS 78439-06-2) serves as an excellent illustration of their importance.

Pharmaceutical reference standards are highly purified substances that act as benchmarks for identifying, quantifying, and testing the quality of drug substances and drug products. They are essential for analytical method development, validation, and routine quality control testing. Without reliable reference standards, ensuring the consistency, potency, and purity of medications would be virtually impossible, jeopardizing patient safety and therapeutic efficacy.

Ceftazidime Pentahydrate, as a well-characterized third-generation cephalosporin antibiotic, is frequently used as a reference standard in the pharmaceutical industry. Laboratories rely on it to:

  • Confirm the identity of Ceftazidime in bulk drug material and finished dosage forms.
  • Quantify the amount of Ceftazidime present in a sample, ensuring it meets specified limits.
  • Assess the purity of the drug substance and identify any impurities.
  • Validate analytical methods used in quality control testing.

The meticulous preparation and certification of reference standards like Ceftazidime Pentahydrate ensure their traceability to official pharmacopeial standards, such as USP or EP. This traceability is critical for regulatory compliance and for ensuring that drugs manufactured globally meet consistent quality benchmarks. By utilizing these standards, manufacturers can confidently release products that are both safe and effective.

The role of compounds like Ceftazidime Pentahydrate as reference standards extends beyond routine testing; they are also vital for research and development. When developing new formulations or investigating drug stability, having a reliable reference point is crucial. NINGBO INNO PHARMCHEM CO.,LTD. is committed to supplying high-quality reference standards that support these critical functions, thereby contributing to the overall quality and safety of pharmaceutical products worldwide.