Pharmaceutical compositions comprising meloxicam and methods...

Chemistry: analytical and immunological testing – Including sample preparation

Reexamination Certificate

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Details

C514S937000, C514S951000, C514S960000, C436S518000, C436S074000

Reexamination Certificate

active

07572641

ABSTRACT:
The present invention encompasses a method of evaluating pharmaceutical compositions of meloxicam whereby one can correlate in vitro properties to in vivo properties, and pharmaceutical compositions developed using the method.

REFERENCES:
patent: 102 50 081 (2004-05-01), None
patent: 0 945 134 (1999-09-01), None
Li, Shoufeng, et al., IV-IVC Consideration in the Development of Immediate-Release Oral Dosage Form, Jul. 2005, Journal of Pharmaceutical Sciences, vol. 94(7), p. 1396-1417.
Odman, J.A.L., et al, The effect of particle size on in vitro dissolution and bioavailability of a low solubility drug, [online], [retrievd on Jun. 26, 2008] Retrieved from the internet <URL:http://www.aapspharmsci.org/abstracts/AM—1999/1843.htm>.
Time stamp of Odman, [online], [retrievd on Jun. 26, 2008] Retrieved from the internet <URL:http://www.aapspharmsci.org/abstracts/AM—1999/>.
Boehringer Ingelheim Internatonal GmbH, Mobic Medicaton Guide, 2004, NDA 20-938/S-004.
Dressman, Jennifer B., In Vitro-in vivo correlaton for lipophilic, poorly water-soluble drugs, 2000, European Journal of Pharmaceutical Sciences, vol. 11 supplimental 2, pp. s73-s80.
Watkins, “Fighting the Clock: Pharmaceutical and biotechnology companies seek ways to reduce the time required to discover and develop medicines”,Chemical and Engineering News, p. 27-34 (Jan. 28, 2002).
United States Pharmacopeia, USP 28/NF23, pp. 2412-15 (2005).
United States Pharmacopeia, USP 28/NF23, pp. 2645 (2005).
Physician's Desk Reference, PDR 58 ed. p. 1016-1019 (Thomson PDR 2004).

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