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Drug Development and Industrial Pharmacy Volume 29, 2003 - Issue 10
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Research Article

Stability Indicating HPTLC Determination of Linezolid as Bulk Drug and in Pharmaceutical Dosage Form

Himani Agrawal Department of Quality Assurance Techniques, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Pune, Maharashtra State, India
, M.Pharm.,
K. R. Mahadik Department of Quality Assurance Techniques, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Pune, Maharashtra State, India
, M.Pharm., Ph.D., F.I.C.A., F.I.C.,
A. R. Paradkar Department of Quality Assurance Techniques, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Pune, Maharashtra State, India
, M.Pharm., Ph.D. &
Neeraj Kaul Department of Quality Assurance Techniques, Poona College of Pharmacy, Bharati Vidyapeeth Deemed University, Pune, Maharashtra State, India
, M.Pharm.
Pages 1119-1126 | Published online: 17 Nov 2003

References

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  • Reddy K.V.S.R., Rao S.M., Suresh T. Isolation and characterization of process-related impurities in linezolid. J. Pharm. Biomed. Anal. 2002; 30: 635–642
  • Alasandro M. Separation of diastereoisomers of DuP 105, a novel oxazolidinone antibacterial agent by supercritical fluid chromatography in a chiral OD column. J. Pharm. Biomed. Anal. 1996; 14: 807–814
  • ICH Q1A. Stability Testing of New Drug Substances and Products. International Conference on Harmonization, Geneva, October, 1993
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  • Sethi P.D. High Performance Thin Layer Chromatography: Quantitative Analysis of Pharmaceutical Formulations. CBS Publishers. 1996; 65–85>

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