Method Development, Validation and Estimation of Relative Response Factor for the Quantitation of Known Impurities in Mometasone Furoate Nasal Spray Dosage form by RP-HPLC with UV/PDA Detector

Author:

Musmade B. D.,Sawant A. V.,Kulkarni S. V.,Nage S. D.,Bhope S. G.,Padmanabhan S.,Lohar K. S.

Publisher

Springer Science and Business Media LLC

Subject

Drug Discovery,Pharmacology

Reference18 articles.

1. ICH (Q3B (R2): Impurity in New Products, Text and Methodology, in: Proceeding of International Conference on Harmonization (June 2006).

2. ICH (Q6A): Specification, Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products, Chemical Substances, in: Proceeding of International Conference on Harmonization (May 2000).

3. P. Ravisankar, S. Gowthami, and G. Devlala Rao, Indian J. Res. Pharm. Biol., 2(3), 1183 – 1195 (2014).

4. C. Roy and J. Chakrabarty, ISRN. Anal. Chem., 2013, 1 – 9 (2013).

5. A. S. Zanwar, D. B. Sen, R. A. Maheshwari, et al., J. Appl. Pharm. Sci., 10(07), 108 – 115 (2020).

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