Advances in orodispersible films for drug delivery

Hariharan M, 2009, Drug Deliv Technol, 9, 24

Barnhart SD, 2008, Modified release drug delivery technology, 2, 209

10.1016/j.ejpb.2009.05.010

Siebenand S, 2010, Pharmazeutische Zeitung, 155, 28

European Medicines Agency. Overview of comments received on draft guideline on the investigation of bioequivalence. CPMP/EWP/QWP/1401/98 REV. 1. London 2010

European Medicines Agency. Guideline on the investigation of bioequivalence. London 2010

10.1016/j.ijpharm.2008.10.002

Garsuch V. Preparation and characterization of fast-dissolving oral films for pediatric use [Doctoral thesis]: Heinrich Heine University, Dusseldorf; 2009

10.1517/13543776.11.6.981

Borsadia SB, 2003, Drug Deliv Technol, 3, 63

10.1016/j.ijpharm.2010.03.055

Patel AR, 2010, Int J Drug Dev Res, 2, 232

10.1016/j.jconrel.2009.06.014

Breitkreutz J, 2010, Innovative Arzneiformen, 37

Mishra R, 2009, Pharm Technol, 33, 48

Peh KK, 1999, J Pharm Pharm Sci, 2, 53

10.1016/j.ejpb.2008.06.032

Corniello CM, 2006, Drug Deliv Technol, 6, 68

Barnhart SD, 2007, Drug Deliv Technol, 7, 34

10.2174/187221108786241660

10.1080/03639040902744704

10.1016/j.ijpharm.2009.07.006

Arya A, 2010, Int J ChemTech Res, 2, 576

10.1201/9780203911532

Koster M, 2010, Annual Meeting of DPhG

10.1016/j.ijpharm.2010.08.010

10.3144/expresspolymlett.2010.92

Malke S, 2010, Int J Pediatr Neonatol, 11

Lehrke I, Vollmer U, Maier S. Primary packaging unit for flat administration forms. WO 2006056161; 2006

10.1517/17425247.4.1.37

Chen MJ, 2008, Drug Deliv Technol, 8, 34

10.1208/s12249-008-9047-7

10.1208/s12249-010-9525-6

10.1016/j.ijpharm.2010.01.008

10.1016/j.ijpharm.2009.05.038

10.2174/156720109789941713

Sharma R, 2007, Indian J Pharm Sci, 69, 320, 10.4103/0250-474X.33174

Ali S, 2007, Drug Deliv Technol, 7, 36

Kulkarni AS, 2010, J Curr Pharm Res, 2, 33

10.1248/cpb.58.454

Garsuch V, 2010, J Pharm Pharmacol, 62, 539, 10.1211/jpp.62.04.0018

10.3109/03639045.2010.505928

Patel R, 2009, Arch Pharm Sci Res, 1, 212

10.1208/s12249-010-9464-2

10.1080/03639040802026012

10.1081/DDC-120021775

10.1081/DDC-43947

Brown D, 2003, Drug Deliv Technol, 3, 58

Gavaskar B, 2010, Int J Pharmacy Pharm Sci, 2, 29

10.1016/j.ijpharm.2008.09.015

10.1016/j.jconrel.2005.01.024

10.1081/DDC-120024178

DIN Deutsches Institut fur Normung. DIN EN ISO 527-1 Bestimmung der Zugeigenschaften Teil 1: Allgemeine Grundsatze. Beuth Verlag GmbH, Berlin; 1996

DIN Deutsches Institut fur Normung. DIN EN ISO 527-3 Bestimmung der Zugeigenschaften Teil 3: Prufbedingungen fur Folien und Tafeln. Beuth Verlag GmbH, Berlin; 2003

10.1016/0378-5173(88)90032-4

European Directorate for the Quality of Medicines & HealthCare. Tablets: Orodispersible Tablets. European Pharmacopoeia 6.8., Strasbourg; 2010. p. 750

10.1248/cpb.44.2121

10.1016/j.ejpb.2009.08.010

Siewert M, 2003, AAPS PharmSciTech, 4, 10.1208/pt040107

10.1517/17425247.5.5.531

Shojaei AH, 1998, J Pharm Pharm Sci, 1, 15

10.14227/DT100203P6

10.1016/j.drudis.2007.01.010

10.1081/DDC-120037481

10.1007/s00216-009-3130-0

10.1016/j.ijpharm.2008.01.036

10.1517/17425247.2.3.507

10.3109/10837450902838700

10.1007/s00702-003-0036-4

10.1007/s00702-003-0042-6