摘要:
A storage stable crystalline Form II of ivabradine hydrochloride having characteristic X-ray powder diffraction peaks at about 15.50°, 18.02°, 19.00°, 19.80°, 22.42°, 24.16°, and 25.46°±0.2° (2¸); comprising a packaging which includes placing crystalline ivabradine hydrochloride in a non-permeable bag; placing the non-permeable bag in polyethylene bag, optionally containing oxygen busters and sealing it; placing the polyethylene bag in a triple laminated bag, optionally containing oxygen busters and sealing it; placing the triple laminated bag inside a high density polyethylene (HDPE) container and sealing it.
摘要:
The invention relates to an improved process for the preparation of etoricoxib and polymorphs thereof. In particular, the, invention relates to a process for the preparation of stable crystalline Form-I of etoricoxib. Further, the invention also relates to a process for the preparation of amorphous form of etoricoxib. The invention also relates to pharmaceutical compositions that include the stable crystalline Form-I of etoricoxib.
摘要:
The present invention provides a process for preparing Ivabradine of formula (I) or its pharmaceutically acceptable salts, solvates, hydrate thereof, by reacting 3-chloro-N-{[(7S)-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl}-N- methylpropan-1 -amine of formula (IV), with 7,8-Dimethoxy-l,3,4,5-tetrahydro-benzo[d]azepin-2-one of formula (V) or its alkaline salt, Formula (V): in presence of base in suitable solvent to provide Ivabradine of formula (I), which can be subsequently converted to its pharmaceutically acceptable salts, solvate or hydrate thereof.
摘要:
A storage stable crystalline Form II of ivabradine hydrochloride having characteristic X-ray powder diffraction peaks at about 15.50°, 18.02°, 19.00°, 19.80°, 22.42°, 24.16°, and 25.46°±0.2° (2θ); comprising a packaging which includes placing crystalline ivabradine hydrochloride in a non-permeable bag; placing the non-permeable bag in polyethylene bag, optionally containing oxygen busters and sealing it; placing the polyethylene bag in a triple laminated bag, optionally containing oxygen busters and sealing it; placing the triple laminated bag inside a high density polyethylene (HDPE) container and sealing it.
摘要:
The present invention provides a process for preparing Ivabradine of formula (I) or its pharmaceutically acceptable salts, solvates, hydrate thereof, by reacting 3-chloro-N-{[(7S)-3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-trien-7-yl]methyl}-N- methylpropan-1 -amine of formula (IV), with 7,8-Dimethoxy-l,3,4,5-tetrahydro-benzo[d]azepin-2-one of formula (V) or its alkaline salt, Formula (V): in presence of base in suitable solvent to provide Ivabradine of formula (I), which can be subsequently converted to its pharmaceutically acceptable salts, solvate or hydrate thereof.
摘要:
The present invention provides pyrroles having hypolipidemic hypocholesteremic activities. The invention provides saroglitazar and its pharmaceutically acceptable salts, hydrates, solvates, polymorphs or intermediates thereof. The invention also provides a process for the preparation of saroglitazar. The invention further provides intermediates as well process for preparation thereof.