These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

282 related items for PubMed ID: 21316175

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. RP-HPLC separation and characterization of unknown impurities of a novel HIV-protease inhibitor Darunavir by ESI-MS and 2D NMR spectroscopy.
    Nageswara Rao R, Ramachandra B, Santhakumar K.
    J Pharm Biomed Anal; 2013 Mar 05; 75():186-91. PubMed ID: 23266664
    [Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Development and validation of a stability indicating RP-HPLC method for the simultaneous determination of related substances of albuterol sulfate and ipratropium bromide in nasal solution.
    Kasawar GB, Farooqui M.
    J Pharm Biomed Anal; 2010 May 01; 52(1):19-29. PubMed ID: 20045275
    [Abstract] [Full Text] [Related]

  • 9. Highly efficient, selective, sensitive and stability indicating RP-HPLC-UV method for the quantitative determination of potential impurities and characterization of four novel impurities in eslicarbazepine acetate active pharmaceutical ingredient by LC/ESI-IT/MS/MS.
    Thomas S, Bharti A, Maddhesia PK, Shandilya S, Agarwal A, Dharamvir, Biswas S, Bhansal V, Gupta AK, Tewari PK, Mathela CS.
    J Pharm Biomed Anal; 2012 Mar 05; 61():165-75. PubMed ID: 22178334
    [Abstract] [Full Text] [Related]

  • 10. A validated stability-indicating RP-HPLC method for levofloxacin in the presence of degradation products, its process related impurities and identification of oxidative degradant.
    Lalitha Devi M, Chandrasekhar KB.
    J Pharm Biomed Anal; 2009 Dec 05; 50(5):710-7. PubMed ID: 19632800
    [Abstract] [Full Text] [Related]

  • 11. Development of a validated RP-LC/ESI-MS-MS method for separation, identification and determination of related substances of tamsulosin in bulk drugs and formulations.
    Nageswara Rao R, Kumar Talluri MV, Narasa Raju A, Shinde DD, Ramanjaneyulu GS.
    J Pharm Biomed Anal; 2008 Jan 07; 46(1):94-103. PubMed ID: 17951020
    [Abstract] [Full Text] [Related]

  • 12. LC determination of glimepiride and its related impurities.
    Khan MA, Sinha S, Vartak S, Bhartiya A, Kumar S.
    J Pharm Biomed Anal; 2005 Oct 04; 39(5):928-43. PubMed ID: 16040224
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. 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 15; 50(3):397-404. PubMed ID: 19541446
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 15.