RP-HPLC Stability Indicating Method Development and Validation of Pseudoephedrine Sulfate and Related Organic Impurities in Tablet Dosage Forms, Robustness by QbD Approach-Reference-Cited by-同舟云学术

RP-HPLC Stability Indicating Method Development and Validation of Pseudoephedrine Sulfate and Related Organic Impurities in Tablet Dosage Forms, Robustness by QbD Approach

Published:2019-09-03 Issue:5 Volume:9 Page:697-710
ISSN:2229-7928
Container-title:Analytical Chemistry Letters
language:en
Short-container-title:Analytical Chemistry Letters

Author:

Dongala Thirupathi¹^ORCID,Katakam Lakshmi Narasimha Rao²,Palakurthi Ashok Kumar¹,Katari Naresh Kumar³^ORCID

Affiliation:

1. Aurex Laboratories LLC, 10 lake drive, East Windsor, NJ, USA 08520

2. Analytical Development, Saptalis Pharmaceuticals LLC, Hauppauge, New York, USA 11788

3. Department of Chemistry, GITAM deemed to be University, Hyderabad, Telangana, India 502329

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/22297928.2019.1696701

Reference24 articles.

1. Simultaneous determination of pseudoephdrine, pheniramine, guaifenisin, pyrilamine, chlorpheniramine and dextromethorphan in cough and cold medicines by high performance liquid chromatography

2. A Quantitative Simultaneous High Performance Liquid Chromatographic Determination of Pseudoephedrine HCl, Guaifenesin and Dextromethorphan HBr.

3. A Porous Graphitized Carbon Column HPLC Method for the Quantification of Paracetamol, Pseudoephedrine, and Chlorpheniramine in a Pharmaceutical Formulation

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