LC/MS for the degradation profiling of cough–cold products under forced conditions-Reference-Cited by-同舟云学术

LC/MS for the degradation profiling of cough–cold products under forced conditions

Published:2004-09 Issue:5 Volume:35 Page:1035-1045
ISSN:0731-7085
Container-title:Journal of Pharmaceutical and Biomedical Analysis
language:en
Short-container-title:Journal of Pharmaceutical and Biomedical Analysis

Author:

Marı́n A.,Barbas C.

Publisher

Elsevier BV

Subject

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

Reference20 articles.

1. ICH topic Q1A(R2). Stability testing of new drug substances and products, 2003. Available on: http://www.hc-sc.gc.ca/hpfb-dgpsa/tpd-dpt/q1a(r2)_e.pdf.

2. ICH topic Q3B(R). Impurities in new drug products, 2003. Available on: http://www.hc-sc.gc.ca/hpfb-dgpsa/tpd-dpt/q3b(r)_e.pdf.

3. Development of validated stability-indicating assay methods—critical review

4. Validation of a HPLC quantification of acetaminophen, phenylephrine and chlorpheniramine in pharmaceutical formulations: capsules and sachets

5. Poly(ethyleneglycol) column for the determination of acetaminophen, phenylephrine and chlorpheniramine in pharmaceutical formulations

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