Stability indicating RP-HPLC method for the determination of Telmisartan in pure and pharmaceutical formulation

International Journal of Pharmacy and Pharmaceutical Sciences

Volumn 3, Issue SUPPL. 2, 2011, Pages 164-167

  Sujana, K ^a   Gowri Sankar, D ^b   Souri, Bala ^c   Swathi Rani, G ^d  

^a ACHARYA NAGARJUNA UNIVERSITY   (India)

^b ANDHRA UNIVERSITY   (India)

^c Neuland Laboratories   (India)

^d NONE

Author keywords

Degradation studies; RP HPLC; Telmisartan

Indexed keywords

PEROXIDE; TELMISARTAN;

ARTICLE; CALIBRATION; CONTROLLED STUDY; DRUG DEGRADATION; DRUG DETERMINATION; DRUG DOSAGE FORM; DRUG FORMULATION; DRUG PURITY; DRUG RETENTION; DRUG STABILITY; FLOW RATE; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; VALIDATION PROCESS;

EID: 80054868520     PISSN: None     EISSN: 09751491     Source Type: Journal    
DOI: None     Document Type: Article

References (11)

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