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Journal of Pharmaceutical Sciences|July 1, 1978
Impurities in drugs II: meperidine and its formulationsK M McErlane, R J Wood, F Matsui, et al.Journal of Pharmaceutical and Biomedical Analysis|January 1, 1989
Validation of a method for the assay of related compounds in famotidine raw materials and formulationsN Beaulieu, S J Graham, R W Sears, et al.Journal of Pharmaceutical Sciences|March 1, 1989
High-performance liquid chromatography method for assay of diltiazem hydrochloride and its related compounds in bulk drug and finished tabletsP M Lacroix, N Beaulieu, T D Cyr, et al.Journal - Association of Official Analytical Chemists|September 1, 1982
Drug quality assessment methods. I. Gas-liquid chromatographic assay and identification of seven barbituratesD B Black, H Kolasinski, E G Lovering, et al.Journal of Pharmaceutical Sciences|April 1, 1980
Identification of degradation products in a phenylbutazone tablet formulationF Matsui, D L Robertson, M A Poirier, et al.Journal - Association of Official Analytical Chemists|March 1, 1985
Liquid chromatographic method for identity, assay, and content uniformity of five tricyclic drugsE G Lovering, N Beaulieu, R C Lawrence, et al.Journal - Association of Official Analytical Chemists|March 1, 1989
Liquid chromatographic methods for vitamins A and D in multivitamin-mineral formulationsN Beaulieu, N M Curran, C Gagné, et al.Journal of Pharmaceutical Sciences|February 1, 1981
Routine quality evaluation of benzodiazepine drugs to USP-NF specificationsD B Black, R C Lawrence, E G Lovering, et al.Journal of Pharmaceutical Sciences|February 1, 1980
Impurities in drugs IV: IndomethacinN M Curran, E G Lovering, K M McErlane, et al.Journal of Pharmaceutical Sciences|September 1, 1979
Impurities in drugs III: TrihexyphenidylM A Poirier, N M Curran, K M McErlane, et al.Pageof 4