Development and validation of a stability indicating HPLC method for determination of lisinopril, lisinopril degradation product and parabens in the lisinopril extemporaneous formulation-Reference-Cited by-同舟云学术

Development and validation of a stability indicating HPLC method for determination of lisinopril, lisinopril degradation product and parabens in the lisinopril extemporaneous formulation

Published:2005-03 Issue:3 Volume:37 Page:559-567
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Beasley Christopher A.,Shaw Jessica,Zhao Zack,Reed Robert A.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry

Reference17 articles.

1. United States Pharmacopeia XXXV, US Pharmcopeial Convention, Rockville, MD.

2. Prinivil®–Merck, Zestril®–AstraZeneca, Prinizide®–Merck and Zestoretic®–AstraZeneca, Product Information, Physician's Desk Reference (PDR), 50th ed., Medical Economics, Monvale, NJ.

3. NDA 19-558 Prinivil (lisinopril) Supplemental New Drug Application, 24 September 2001.

4. Spectrophotometric, septrofluorimetric and LC determination of lisinopril

5. Spectrophotometric determination of lisinopril in tablets using 1-fluoro-2,4-dinitrobenzene reagent

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