207 related articles for article (PubMed ID: 34463320)
21. Development of a stability- indicating HPLC method for simultaneous determination of ten related substances in vonoprazan fumarate drug substance.
Luo Z; Liu A; Liu Y; Wang G; Chen X; Wang H; Li M; Zhang H; Qiu Y; Zhai H
J Pharm Biomed Anal; 2018 Feb; 149():133-142. PubMed ID: 29112902
[TBL] [Abstract][Full Text] [Related]
22. A Stability-Indicating UPLC Method for the Determination of Potential Impurities and Its Mass by a New QDa Mass Detector in Daclatasvir Drug Used to Treat Hepatitis C Infection.
Jagadabi V; Nagendra Kumar PV; Mahesh K; Pamidi S; Ramaprasad LA; Nagaraju D
J Chromatogr Sci; 2019 Jan; 57(1):44-53. PubMed ID: 30169761
[TBL] [Abstract][Full Text] [Related]
23. Development and validation of an UPLC method for rapid determination of ibuprofen and diphenhydramine citrate in the presence of impurities in combined dosage form.
Rao DD; Sait SS; Mukkanti K
J Chromatogr Sci; 2011 Apr; 49(4):281-6. PubMed ID: 21439118
[TBL] [Abstract][Full Text] [Related]
24. Quantification of potential impurities by a stability indicating UV-HPLC method in niacinamide active pharmaceutical ingredient.
Thomas S; Bharti A; Tharpa K; Agarwal A
J Pharm Biomed Anal; 2012 Feb; 60():86-90. PubMed ID: 22115882
[TBL] [Abstract][Full Text] [Related]
25. Stability-indicating LC-UV method for the determination of eszopiclone and degradation impurities in tablet dosage form.
Shaikh K; Patil A; Gite S
J Chromatogr Sci; 2014 Apr; 52(4):293-7. PubMed ID: 23552846
[TBL] [Abstract][Full Text] [Related]
26. Development and validation of a reversed-phase ultra-performance liquid chromatographic method for assay of lacidipine and related substances.
Mohan A; Patel HB; Saravanan D
J AOAC Int; 2011; 94(6):1800-6. PubMed ID: 22320087
[TBL] [Abstract][Full Text] [Related]
27. Development of validated stability indicating assay method for simultaneous estimation of metformin hydrochloride and vildagliptin by RP-HPLC.
Satheeshkumar N; Pradeepkumar M; Shanthikumar S; Rao VJ
Drug Res (Stuttg); 2014 Mar; 64(3):124-9. PubMed ID: 24081820
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. Stability-indicating HPLC method for quantification of celecoxib and diacerein along with its impurities in capsule dosage form.
Bapatu HR; Maram RK; Murthy RS
J Chromatogr Sci; 2015 Jan; 53(1):144-53. PubMed ID: 24837233
[TBL] [Abstract][Full Text] [Related]
30. A validated stability-indicating LC method for acetazolamide in the presence of degradation products and its process-related impurities.
Srinivasu P; Subbarao DV; Vegesna RV; Sudhakar Babu K
J Pharm Biomed Anal; 2010 May; 52(1):142-8. PubMed ID: 20053517
[TBL] [Abstract][Full Text] [Related]
31. Quality by design approach for the separation of naproxcinod and its related substances by fused core particle technology column.
Inugala UR; Pothuraju NR; Vangala RR
J Chromatogr Sci; 2013; 51(5):453-9. PubMed ID: 23060406
[TBL] [Abstract][Full Text] [Related]
32. Development and validation of a stability-indicating assay method for simultaneous determination of perindopril and indapamide in combined dosage form by reversed-phase high-performance liquid chromatography.
Jogia H; Khandelwal U; Gandhi T; Singh S; Modi D
J AOAC Int; 2010; 93(1):108-15. PubMed ID: 20334172
[TBL] [Abstract][Full Text] [Related]
33. Robust and Rugged Stability-Indicating HPLC Method for the Determination of Plerixafor and Its Related Impurities in Drug Substances.
Bapatu HR; Maram RK; Murthy RS
J Chromatogr Sci; 2015 Oct; 53(9):1432-42. PubMed ID: 25858970
[TBL] [Abstract][Full Text] [Related]
34. Development and Validation of a Stability-Indicating RP-HPLC Method for the Determination of Process-Related Impurities and Degradation Products of Rabeprazole Sodium in Pharmaceutical Formulation.
Kumar N; Sangeetha D
Sci Pharm; 2013; 81(3):697-711. PubMed ID: 24106668
[TBL] [Abstract][Full Text] [Related]
35. Quantification of halobetasol propionate and its impurities present in topical dosage forms by stability-indicating LC method.
Nalwade S; Reddy VR; Kulkarni D; Todamal S
J Chromatogr Sci; 2015 Jan; 53(1):127-34. PubMed ID: 24784115
[TBL] [Abstract][Full Text] [Related]
36. A stability-indicating reversed-phase high-performance liquid chromatography method for Ambrisentan: an endothelin receptor antagonist.
Satheeshkumar N; Naveenkumar G
J Chromatogr Sci; 2014 Sep; 52(8):894-8. PubMed ID: 24042432
[TBL] [Abstract][Full Text] [Related]
37. A validated stability-indicating normal phase LC method for clopidogrel bisulfate and its impurities in bulk drug and pharmaceutical dosage form.
Durga Rao D; Kalyanaraman L; Sait SS; Venkata Rao P
J Pharm Biomed Anal; 2010 May; 52(1):160-5. PubMed ID: 20074888
[TBL] [Abstract][Full Text] [Related]
38. A stability-indicating ultra-performance liquid chromatographic method for estimation of related substances and degradants in paliperidone active pharmaceutical ingredient and its pharmaceutical dosage forms.
Bindu KH; Reddy IU; Anjaneyulu Y; Suryanarayana MV
J Chromatogr Sci; 2012 Apr; 50(4):368-72. PubMed ID: 22407348
[TBL] [Abstract][Full Text] [Related]
39. Simultaneous Determination of Impurities of Atazanavir and Ritonavir in Tablet Dosage Form by Using Reversed-Phase Ultra Performance Liquid Chromatographic Method.
Mantripragada MKVVN; Rao SV; Nutulapati VVS; Mantena BPV
J Chromatogr Sci; 2018 Mar; 56(3):270-284. PubMed ID: 29300835
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]