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0033806376
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The reason for an increase in decomposition of rifampicin in the presence of isoniazid under acid conditions
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Singh S, Mariappan T T, Sharda N, Kumar S, Chakraborti A K. The reason for an increase in decomposition of rifampicin in the presence of isoniazid under acid conditions. Pharm Pharmacol Commun 2000; 6: 405-410.
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0033659569
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Degradation of rifampicin, isoniazid and pyrazinamide from prepared mixtures and marketed single and combination products under acid conditions
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Singh S, Mariappan T T, Sharda N, Singh B. Degradation of rifampicin, isoniazid and pyrazinamide from prepared mixtures and marketed single and combination products under acid conditions. Pharm Pharmacol Commun 2000; 6: 491-494.
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0035834176
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A critical review of the probable reasons for the variable bioavailability of rifampicin from anti-tuberculosis fixed-dose combination (FDC) products, and the likely solutions to the problem
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Singh S, Mariappan T T, Shankar R, Sharda N, Singh B. A critical review of the probable reasons for the variable bioavailability of rifampicin from anti-tuberculosis fixed-dose combination (FDC) products, and the likely solutions to the problem. Int J Pharm 2001; 228: 5-17.
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0034847472
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Efforts of the WHO/IUATLD to solve the problem of poor bioavailability of rifampicin from FDC anti-tuberculosis products: Is a change required in the direction of the approach in the view of recent findings?
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Singh S. Efforts of the WHO/IUATLD to solve the problem of poor bioavailability of rifampicin from FDC anti-tuberculosis products: is a change required in the direction of the approach in the view of recent findings? Int J Tuberc Lung Dis 2001; 5: 880-882.
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Recent bioequivalence studies on fixed dose combination anti tuberculosis drug formulations available on the global market
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Pillai G, Fourie P B, Padayatchi N, et al. Recent bioequivalence studies on fixed dose combination anti tuberculosis drug formulations available on the global market. Int J Tuberc Lung Dis 1999; 3 (Suppl 3): S309-S316.
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Bioequivalence study of rifampicin in fixed dose combination of rifampicin and isoniazid vs. separate formulations
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Panchagnula R, Singh I, Kaur K J, Kaul C L. Bioequivalence study of rifampicin in fixed dose combination of rifampicin and isoniazid vs. separate formulations. Methods Find Exp Clin Pharmacol 1999; 21: 625-628.
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0032759650
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The WHO simplified study protocol in practice: Investigation of combined formulations supplied by the WHO
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Panchagnula R, Kaur K J, Singh I, Kaul C L. The WHO simplified study protocol in practice: investigation of combined formulations supplied by the WHO. Int J Tuberc Lung Dis 1999; 3 (Suppl 3): S336-S342.
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0012572533
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Q1AR. Geneva: ICH
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The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use. Stability testing of new drug substances and products. Q1AR. Geneva: ICH, 2000.
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Stability Testing of New Drug Substances and Products
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Quality assurance of fixed-dose combinations of anti-tuberculosis medications
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Proceedings of an IUATLD/WHO workshop
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Quality assurance of fixed-dose combinations of anti-tuberculosis medications. Proceedings of an IUATLD/WHO workshop. Int J Tuberc Lung Dis 1999; 3 (Suppl 3): S281-S387.
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Permeation of unit-dose blister market containers under USP and ICH conditions
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Taborsky C J, Foster M G, Lockhart H, Polgar B. Permeation of unit-dose blister market containers under USP and ICH conditions. Pharm Tech 2000; 24: 38-42.
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