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Volumn 57, Issue 5, 2009, Pages 534-541
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Development of a validated RP-HPLC method for separation and determination of process-related impurities of omeprazole in bulk drugs
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Author keywords
Omeprazole; Process related impurities; RP HPLC; Validation
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Indexed keywords
2 [(3,5 DIMETHYLPYRIDIN 2 YL)METHYL]SULPHINYL 5 METHOXY 1H BENZIMIDAZOLE;
4 METHOXY 2 [[(5 METHOXY 1H BENZIMIDAZOL 2 YL)SULPHINYL]METHYL] 3,5 DIMETHYLPYRIDINE 1 OXIDE;
5 METHOXY 1H BENZIMIDAZOLE 2 THIOL;
5 METHOXY 2 [[(4 CHLORO 3,5 DIMETHYLPYRIDIN 2 YL)METHYL]SULPHINYL] 1H BENZIMIDAZOLE;
BENZIMIDAZOLE DERIVATIVE;
OMEPRAZOLE;
OMEPRAZOLE SULFONE;
UFIPRAZOLE;
UNCLASSIFIED DRUG;
ACCURACY;
ARTICLE;
CALIBRATION;
DRUG IMPURITY;
DRUG STRUCTURE;
LIQUID CHROMATOGRAPHY;
PH;
REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY;
SEPARATION TECHNIQUE;
ULTRAVIOLET RADIATION;
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EID: 73349117471
PISSN: 00148237
EISSN: None
Source Type: Journal
DOI: None Document Type: Article |
Times cited : (15)
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References (5)
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