Evaluation of influence of different manufacturing technologies on impurity profile of immediate release formulation comprising highly degradable ACE inhibitor as model active substance
Author:
Affiliation:
1. Research & Development, Alkaloid AD Skopje, Blvd. Aleksandar Makedonski 12, 1000 Skopje, North Macedonia
Publisher
Macedonian Pharmaceutical Association
Subject
General Medicine
Link
https://bulletin.mfd.org.mk/volumes/Volume%2068_3/68_3_145.pdf
Reference3 articles.
1. Kovaleski, J., Kraut, B., Mattiuz, A., Giangiulio, M., Brobst, G., Cagno, W., Kulkarni, P. and Rauch, T., 2007. Impurities in generic pharmaceutical development☆. Advanced Drug Delivery Reviews 59(1), 56-63. https://doi.org/10.1016/j.addr.2006.10.009
2. Qiu, F. and Norwood, D., 2007. Identification of Pharmaceutical Impurities. Journal of Liquid Chromatography & Related Technologies 30(5-7), 877-935. https://doi.org/10.1080/10826070701191151
3. Regulska, K., Stanisz, B. and Lisiecki, P., 2013. Optimization of Storage and Manufacture Conditions for Imidapril Hydrochloride in Solid State as a Way to Reduce Costs of Antihypertensive Therapy. AAPS PharmSciTech 14(3), 1199-1208. https://doi.org/10.1208/s12249-013-0010-x
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