112 related articles for article (PubMed ID: 24082357)
1. Stability-indicating Method for the Estimation of Riluzole in Tablets.
Neeha T; Bhargavi P; Jyothi AA; Devalarao G; Nalluri BN
Indian J Pharm Sci; 2013 May; 75(3):372-6. PubMed ID: 24082357
[TBL] [Abstract][Full Text] [Related]
2. High-Performance Liquid Chromatography and Liquid Chromatography/Mass Spectrometry Studies on Stress Degradation Behavior of Sulfapyridine and Development of a Validated, Specific, Stability-Indicating HPLC Assay Method.
Kapoor B; Gupta R; Gulati M; Singh SK; Khatik GL; Chawla M; Nagappan KV; Khursheed R; Kumar R
Assay Drug Dev Technol; 2020 Apr; 18(3):119-133. PubMed ID: 32267712
[TBL] [Abstract][Full Text] [Related]
3. Stability-indicating RP-HPLC Method for the Simultaneous Determination of Sitagliptin and Simvastatin in Tablets.
Ramalingam P; Bhaskar VU; Reddy YP; Kumar KV
Indian J Pharm Sci; 2014 Sep; 76(5):407-14. PubMed ID: 25425754
[TBL] [Abstract][Full Text] [Related]
4. Stability-indicating HPLC method development and validation for simultaneous estimation of metformin, dapagliflozin, and saxagliptin in bulk drug and pharmaceutical dosage form.
Vankalapati KR; Alegete P; Boodida S
Biomed Chromatogr; 2022 Jul; 36(7):e5384. PubMed ID: 35434817
[TBL] [Abstract][Full Text] [Related]
5. A validated stability-indicating liquid chromatographic method for determination of degradation impurities and diastereomers in voriconazole tablets.
Shaikh KA; Patil AT
Sci Pharm; 2012; 80(4):879-88. PubMed ID: 23264937
[TBL] [Abstract][Full Text] [Related]
6. Stability-indicating liquid chromatographic method for the quantification of the new antipsychotic agent asenapine in bulk and in pharmaceutical formulation.
Chhalotiya UK; Bhatt KK; Shah DA; Patel JR
Sci Pharm; 2012; 80(2):407-17. PubMed ID: 22896826
[TBL] [Abstract][Full Text] [Related]
7. RP-HPLC method for simultaneous estimation of bisoprolol fumarate and hydrochlorothiazide in tablet formulation.
Joshi SJ; Karbhari PA; Bhoir SI; Bindu KS; Das C
J Pharm Biomed Anal; 2010 Jul; 52(3):362-71. PubMed ID: 19926421
[TBL] [Abstract][Full Text] [Related]
8. LC and LC-MS/MS study of forced decomposition behavior of anastrozole and establishment of validated stability-indicating analytical method for impurities estimation in low dose anastrozole tablets.
Reddy YR; Nandan SR; Bharathi DV; Nagaraju B; Reddy SS; Ravindranath LK; Rao VS
J Pharm Biomed Anal; 2009 Oct; 50(3):397-404. PubMed ID: 19541446
[TBL] [Abstract][Full Text] [Related]
9. [Impurity profile of macitentan in tablet dosage form using a stability-indicating high performance liquid chromatography method and forced degradation study].
Lakka NS; Kuppan C; Rangasamy P
Se Pu; 2019 Jan; 37(1):100-110. PubMed ID: 30693716
[TBL] [Abstract][Full Text] [Related]
10. Development and Validation of Stability Indicating RP-HPLC Method for Voriconazole.
Khetre AB; Sinha PK; Damle MC; Mehendre R
Indian J Pharm Sci; 2009 Sep; 71(5):509-14. PubMed ID: 20502568
[TBL] [Abstract][Full Text] [Related]
11. Development and Validation of a Stability Indicating RP-HPLC Method for Simultaneous Estimation of Teneligliptin and Metformin.
Vetapalem R; Yejella RP; Atmakuri LR
Turk J Pharm Sci; 2020 Apr; 17(2):141-147. PubMed ID: 32454773
[TBL] [Abstract][Full Text] [Related]
12. Validation of a Stability-Indicating RP-HPLC Method for the Simultaneous Determination of Trimethoprim and Sulfadimethoxine Sodium in Oral Liquid Dosage Form.
Ghanem MM; Abu-Lafi SA
Sci Pharm; 2013; 81(2):459-74. PubMed ID: 23833713
[TBL] [Abstract][Full Text] [Related]
13. Rapid Estimation of Tadalafil by Reverse-phase High-performance Liquid Chromatography Method in Bulk and Tablet Formulation.
Sonawane PH; Panzade PS; Kale MA
Indian J Pharm Sci; 2013 Mar; 75(2):230-3. PubMed ID: 24019575
[TBL] [Abstract][Full Text] [Related]
14. Stability Indicating RP-HPLC Estimation of Nebivolol Hydrochloride in Pharmaceutical Formulations.
Shah DA; Bhatt KK; Mehta RS; Baldania SL; Gandhi TR
Indian J Pharm Sci; 2008 Sep; 70(5):591-5. PubMed ID: 21394254
[TBL] [Abstract][Full Text] [Related]
15. UPLC and LC-MS studies on degradation behavior of irinotecan hydrochloride and development of a validated stability-indicating ultra-performance liquid chromatographic method for determination of irinotecan hydrochloride and its impurities in pharmaceutical dosage forms.
Kumar N; Sangeetha D; Reddy SP
J Chromatogr Sci; 2012 Oct; 50(9):810-9. PubMed ID: 22661461
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Stability-indicating HPLC method for determination of fosamprenavir calcium.
Chilukuri M; Narayanareddy P; Hussianreddy K
J Chromatogr Sci; 2014 Sep; 52(8):781-7. PubMed ID: 23893948
[TBL] [Abstract][Full Text] [Related]
18. Development of a Stability-Indicating RP-UPLC Method for Rapid Determination of Metaxalone and its Degradation Products in Solid Oral Dosage Form.
Trivedi RK; Patel MC
Sci Pharm; 2012; 80(2):353-66. PubMed ID: 22896822
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Riluzole: validation of stability-indicating HPLC, D1 and DD1 spectrophotometric assays.
Saleh OA; El-Azzouny AA; Aboul-Enein HY; Badawey AM
J Chromatogr Sci; 2014 Jul; 52(6):539-46. PubMed ID: 23744878
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
