264 related articles for article (PubMed ID: 21617775)
21. Impurity profiling and a stability-indicating UPLC method development and validation for the estimation of related impurities of halobetasol propionate in halobetasol propionate 0.05% (w/w) cream.
Prakash L; Malipeddi H; Subbaiah BV; Lakka NS
J Chromatogr Sci; 2015 Jan; 53(1):112-21. PubMed ID: 24795078
[TBL] [Abstract][Full Text] [Related]
22. A Novel, Validated Stability-Indicating UPLC Method for the Estimation of Lansoprazole and its Impurities in Bulk Drug and Pharmaceutical Dosage Forms.
Rao PV; Kumar MN; Kumar MR
Sci Pharm; 2013; 81(1):183-93. PubMed ID: 23641337
[TBL] [Abstract][Full Text] [Related]
23. Identification and Characterization of an Oxidative Degradation Product of Fexofenadine, Development and Validation of a Stability-Indicating RP-UPLC Method for the Estimation of Process Related Impurities and Degradation Products of Fexofenadine in Pharmaceutical Formulations.
Vaghela B; Rao SS; Reddy AM; Venkatesh P; Kumar N
Sci Pharm; 2012; 80(2):295-309. PubMed ID: 22896817
[TBL] [Abstract][Full Text] [Related]
24. A novel validated stability indicating high performance liquid chromatographic method for estimation of degradation behavior of ciprofloxacin and tinidazole in solid oral dosage.
Vaghela BK; Rao SS
J Pharm Bioallied Sci; 2013 Oct; 5(4):298-308. PubMed ID: 24302838
[TBL] [Abstract][Full Text] [Related]
25. Development and validation of a stability-indicating RP-LC method for famciclovir.
Raman NV; Harikrishna KA; Prasad AV; Ratnakar Reddy K; Ramakrishna K
J Pharm Biomed Anal; 2009 Dec; 50(5):797-802. PubMed ID: 19632799
[TBL] [Abstract][Full Text] [Related]
26. A Stability Indicating Method for the Determination of the Antioxidant Sodium Bisulfite in Pharmaceutical Formulation by RP-HPLC Technique.
Trivedi HK; Patel MC
Sci Pharm; 2011; 79(4):909-20. PubMed ID: 22145114
[TBL] [Abstract][Full Text] [Related]
27. A Novel, Rapid, and Validated Stability-Indicating UPLC Method for the Estimation of Drotaverine Hydrochloride and Ibuprofen Impurities in Oral Solid Dosage Form.
Vijay Kumar R; Rao VU; Anil Kumar N; Venkata Subbaiah B
Sci Pharm; 2015; 83(4):567-81. PubMed ID: 26839839
[TBL] [Abstract][Full Text] [Related]
28. A Rapid, Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Formoterol Fumarate, Tiotropium Bromide, and Ciclesonide in a Pulmonary Drug Product.
Trivedi RK; Chendake DS; Patel MC
Sci Pharm; 2012; 80(3):591-603. PubMed ID: 23008808
[TBL] [Abstract][Full Text] [Related]
29. A new, rapid, stability-indicating UPLC method for separation and determination of impurities in amlodipine besylate, valsartan and hydrochlorothiazide in their combined tablet dosage form.
Vojta J; Jedlička A; Coufal P; Janečková L
J Pharm Biomed Anal; 2015 May; 109():36-44. PubMed ID: 25756663
[TBL] [Abstract][Full Text] [Related]
30. Validated Stability-indicating High-performance Liquid Chromatographic Method for Estimation of Degradation Behaviour of Eberconazole Nitrate and Mometasone Furoate in Cream Formulation.
Sharma N; Rao SS; Vaghela B
Indian J Pharm Sci; 2013 Jan; 75(1):76-82. PubMed ID: 23901164
[TBL] [Abstract][Full Text] [Related]
31. A novel stability-indicating UPLC method development and validation for the determination of seven impurities in various diclofenac pharmaceutical dosage forms.
Azougagh M; Elkarbane M; Bakhous K; Issmaili S; Skalli A; Iben Moussad S; Benaji B
Ann Pharm Fr; 2016 Sep; 74(5):358-69. PubMed ID: 27475309
[TBL] [Abstract][Full Text] [Related]
32. Development and validation of a simple, sensitive, selective and stability-indicating RP-UPLC method for the quantitative determination of ritonavir and its related compounds.
Koppala S; Panigrahi B; Raju SV; Padmaja Reddy K; Ranga Reddy V; Anireddy JS
J Chromatogr Sci; 2015; 53(5):662-75. PubMed ID: 25186277
[TBL] [Abstract][Full Text] [Related]
33. Development and Validation of a Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Phenoxyethanol, Methylparaben, Propylparaben, Mometasone Furoate, and Tazarotene in Topical Pharmaceutical Dosage Formulation.
Roy C; Chakrabarty J
Sci Pharm; 2013; 81(4):951-67. PubMed ID: 24482766
[TBL] [Abstract][Full Text] [Related]
34. Evaluation of Perampanel in the Presence of its Degradation Products and Process-Related Impurities by Validated Stability-Indicating Reverse Phase High Performance Liquid Chromatography Method.
Varghese SJ; Mohanakishore G; Ravi TK
J Chromatogr Sci; 2022 Jul; 60(6):571-577. PubMed ID: 34463320
[TBL] [Abstract][Full Text] [Related]
35. A developed and validated stability-indicating reverse-phase high performance liquid chromatographic method for determination of cefdinir in the presence of its degradation products as per International Conference on Harmonization guidelines.
Hamrapurkar P; Patil P; Phale M; Gandhi M; Pawar S
Pharm Methods; 2011 Jan; 2(1):15-20. PubMed ID: 23781424
[TBL] [Abstract][Full Text] [Related]
36. Development and Validation of a Stability-indicating UPLC-DAD Method for the Simultaneous Determination of Ivermectin and Praziquantel in Pharmaceutical Tablets and Dissolution Media.
Ibrahim A; Wang F; Gary Hollenbeck R; Martinez MN; Fahmy R; Hoag SW
AAPS PharmSciTech; 2023 Oct; 24(7):211. PubMed ID: 37821763
[TBL] [Abstract][Full Text] [Related]
37. Identification of Degradation Products and a Stability-Indicating RP-HPLC Method for the Determination of Flupirtine Maleate in Pharmaceutical Dosage Forms.
Peraman R; Lalitha KV; Raja NM; Routhu HB
Sci Pharm; 2014; 82(2):281-93. PubMed ID: 24959399
[TBL] [Abstract][Full Text] [Related]
38. A fast, stability-indicating, and validated liquid chromatography method for the purity control of lercanidipine hydrochloride in tablet dosage form.
Mehta S; Singh S; Chikhalia K
Sci Pharm; 2014; 82(2):327-40. PubMed ID: 24959405
[TBL] [Abstract][Full Text] [Related]
39. A validated stability-indicating LC method for the separation of enantiomer and potential impurities of Linezolid using polar organic mode.
Satyanarayana Raju T; Vishweshwari Kutty O; Ganesh V; Yadagiri Swamy P
J Pharm Anal; 2012 Aug; 2(4):272-278. PubMed ID: 29403753
[TBL] [Abstract][Full Text] [Related]
40. Development and Validation of a Stability-Indicating High-Performance Liquid Chromatographic Method for the Quantification of Methocarbamol and Its Impurities in Pharmaceutical Dosage Forms.
Kalokhe S; Nalwade S; Patil P; Raskar P
J Chromatogr Sci; 2021 May; 59(6):555-565. PubMed ID: 33395699
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]