Takagi, T.; Masada, T.; Minami, K.; Kataoka, M.; Yamashita, S.
Development of an In Vitro Methodology to Assess the Bioequivalence of Orally Disintegrating Tablets Taken without Water. Pharmaceutics 2023, 15, 2192.
https://doi.org/10.3390/pharmaceutics15092192
AMA Style
Takagi T, Masada T, Minami K, Kataoka M, Yamashita S.
Development of an In Vitro Methodology to Assess the Bioequivalence of Orally Disintegrating Tablets Taken without Water. Pharmaceutics. 2023; 15(9):2192.
https://doi.org/10.3390/pharmaceutics15092192
Chicago/Turabian Style
Takagi, Toshihide, Takato Masada, Keiko Minami, Makoto Kataoka, and Shinji Yamashita.
2023. "Development of an In Vitro Methodology to Assess the Bioequivalence of Orally Disintegrating Tablets Taken without Water" Pharmaceutics 15, no. 9: 2192.
https://doi.org/10.3390/pharmaceutics15092192
APA Style
Takagi, T., Masada, T., Minami, K., Kataoka, M., & Yamashita, S.
(2023). Development of an In Vitro Methodology to Assess the Bioequivalence of Orally Disintegrating Tablets Taken without Water. Pharmaceutics, 15(9), 2192.
https://doi.org/10.3390/pharmaceutics15092192