Stability of loratadine tablets in Argentina
Brevedan, Marta I. V. et al · SEDICI UNLP · 2011
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tablets available in Argentina were assessed. Drug content and dissolution profiles were determined according to USP29, at time zero, and after 3 and 6 months of storage under ICH accelerated aging conditions (40 °C, 75 % RH). Dissolution efficiency and assay values were compared, both by mathematical and
statistical methods, to assess interchangeability and stability during aging. After 180 days, most formulations evaluated showed statistically significant changes in the active ingredient and in the dissolution behaviour. Only formulation K did not meet the assay acceptance criteria.
Colegio de Farmacéuticos de la Provincia de Buenos Aires
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APA 7
Brevedan, M. I. V. E. A. (2011). Stability of loratadine tablets in Argentina. http://sedici.unlp.edu.ar/handle/10915/8202
MLA
Brevedan, Marta I. V. et al. "Stability of loratadine tablets in Argentina." 2011. http://sedici.unlp.edu.ar/handle/10915/8202.
Chicago
Brevedan, Marta I. V. et al. 2011. "Stability of loratadine tablets in Argentina.". http://sedici.unlp.edu.ar/handle/10915/8202.
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Brevedan, M. I. V. E. A. 2011, Stability of loratadine tablets in Argentina, SEDICI UNLP, available at: http://sedici.unlp.edu.ar/handle/10915/8202 [Accessed 25 Jun. 2026].
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- Título
- Stability of loratadine tablets in Argentina
- Autor / colaboradores
- Brevedan, Marta I. V. et al
- Editorial
- SEDICI UNLP
- Año de publicación
- 2011
- Idioma
- en
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