Author:
Veiga Andressa,Oliveira Paulo R.,Bernardi Larissa S.,Mendes Cassiana,Silva Marcos A. S.,Sangoi Maximiliano S.,Janissek Paulo R.,Murakami Fábio S.
Publisher
Springer Science and Business Media LLC
Reference31 articles.
1. Gandhi R, Pillai O, Thilagavathi R, Gopalakrishnan B, Kaul CL, Panchagnula R. Characterization of azithromycin hydrates. Eur J Pharm Sci. 2002;16(3):175–84.
2. Tomassetti M, Catalani A, Rossi V, Vecchio S. Thermal analysis study of the interactions between acetaminophen and excipients in solid dosage forms and in some binary mixtures. J Pharm Biomed Anal. 2005;37(5):949–55.
3. Patel P, Ahir K, Patel V, Manani L, Patel C. Drug-excipient compatibility studies: first step for dosage form development. Pharm Innov J. 2015;4(5):14–20.
4. Ahuja S. Assuring quality of drugs by monitoring impurities. Adv Drug Deliv Rev. 2007;59(1):3–11.
5. Kovaleski J, Kraut B, Mattiuz A, Giangiulio M, Brobst G, Cagno W, Kulkarni P, Rauch T. Impurities in generic pharmaceutical development. Adv Drug Deliv Rev. 2007;59(1):56–63.
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