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Items: 1 to 20 of 270

2.

A Validated Stability-Indicating RP-UPLC Method for Simultaneous Determination of Desloratadine and Sodium Benzoate in Oral Liquid Pharmaceutical Formulations.

Kumar N, Sangeetha D, Reddy PS, Prakash L.

Sci Pharm. 2012;80(1):153-65. doi: 10.3797/scipharm.1111-08. Epub 2011 Dec 12.

3.

Stress degradation studies and development of a validated stability-indicating-assay-method for determination of diacerein in presence of degradation products.

Hamrapurkar P, Patil P, Desai M, Phale M, Pawar S.

Pharm Methods. 2011 Jan;2(1):30-5. doi: 10.4103/2229-4708.81088.

4.

Development and validation of a stability indicating RP-UPLC method for determination of quetiapine in pharmaceutical dosage form.

Trivedi RK, Patel MC.

Sci Pharm. 2011 Mar;79(1):97-111. doi: 10.3797/scipharm.1009-12. Epub 2011 Jan 16.

5.

A Rapid Stability-Indicating RP-HPLC Method for the Determination of Betaxolol Hydrochloride in Pharmaceutical Tablets.

Auvity S, Chiadmi F, Cisternino S, Fontan JE, Schlatter J.

Anal Chem Insights. 2013;8:1-7. doi: 10.4137/ACI.S11256. Epub 2013 Mar 11.

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11.

Method Development and Validation of a Stability-Indicating RP-HPLC Method for the Quantitative Analysis of Dronedarone Hydrochloride in Pharmaceutical Tablets.

Dabhi B, Jadeja Y, Patel M, Jebaliya H, Karia D, Shah A.

Sci Pharm. 2013 Mar;81(1):115-22. doi: 10.3797/scipharm.1209-15. Epub 2012 Nov 5.

12.

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. doi: 10.3797/scipharm.1104-13. Epub 2011 Aug 7.

13.

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 Jun;80(2):353-66. doi: 10.3797/scipharm.1112-08. Epub 2012 Feb 21.

15.

Development and Validation of Stability-indicating HPLC Method for Betamethoasone Dipropionate and Related Substances in Topical Formulation.

Vairale AS, Sivaswaroop P, Bandana S.

Indian J Pharm Sci. 2012 Mar;74(2):107-15. doi: 10.4103/0250-474X.103840.

16.

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 Jun;80(2):407-17. doi: 10.3797/scipharm.1112-07. Epub 2012 Apr 1.

18.

Simultaneous determination of cefdinir and cefixime in human plasma by RP-HPLC/UV detection method: Method development, optimization, validation, and its application to a pharmacokinetic study.

Khan A, Iqbal Z, Khan MI, Javed K, Khan A, Ahmad L, Shah Y, Nasir F.

J Chromatogr B Analyt Technol Biomed Life Sci. 2011 Aug 15;879(24):2423-9. doi: 10.1016/j.jchromb.2011.06.040. Epub 2011 Jul 6.

PMID:
21782531
19.

Stress degradation studies on varenicline tartrate and development of a validated stability-indicating HPLC method.

Pujeri SS, Khader AM, Seetharamappa J.

Sci Pharm. 2012;80(1):115-26. doi: 10.3797/scipharm.1109-22. Epub 2011 Dec 5.

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