Abstract:
The present invention relates to oral liquid pharmaceutical compositions that include sertraline. The invention also relates to processes for the preparation of the pharmaceutical compositions and their use in treating medical conditions. The oral liquid pharmaceutical composition includes sertraline or a pharmaceutically acceptable salt thereof and water. The water is present at an amount that is greater than about 10% w/w to about 40% w/w of the composition.
Abstract:
The present invention relates to stable oral benzimidazole compositions and processes for their preparation. The stable oral benzimidazole pharmaceutical composition includes a core, a separating layer, and an enteric coating. The core includes a benzimidazole compound, a substantially water-soluble material and, optionally, one or more pharmaceutically acceptable excipients, wherein the core is not alkaline. The separating layer surrounds the core and includes a substantially water-soluble material and, optionally, one or more pharmaceutically acceptable excipients. The enteric coating surrounds the separating layer. At least one of the core and the separating layer includes the substantially water-soluble material without any pharmaceutically acceptable excipients.
Abstract:
In accordance with an example embodiment a method and apparatus is provided. The method comprises receiving at least one face as an input. A presence of the at least one face in a media content is determined and a modified display of the media content is generated if the at least one face is determined to be present in the media content.
Abstract:
The invention provides a process for preparing 3 -hydroxy-1-(3- (trifluoromethyl)-5,6-dihydro-[l,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl)-4-(2,4,5-trifluorophenyl) butan-1-one (Formula I), into its racemic (R/S) form or any of its optically active (S) or (R) forms or enantiomeric excess mixture of any of the forms comprising: a) reacting 4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1- (2,4,5-trifluorophenyl)butan-2-one of formula (III) with a suitable oxidoreductase enzymes or its suitable variants in the presence of suitable conditions and co-factor b) isolating 3-hydroxy-1-(3-(trifluoromethyl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazin- 7(8H)-yl)-4-(2,4,5-trifluorophenyl) butan-1-one, into its racemic (R/S) form or any of its optically active (S) or (R) forms or enantiomeric excess mixture of any of the forms
Abstract:
The present invention relates to a process for the preparation of optically pure (S,S)-6-t-butoxycarbonyl-hexahydro-1-pyridazinylcarbonyl-1,3-dioxo-2-isoindolebutyric acid, an intermediate for the preparation of cilazapril.
Abstract:
A detergent bar comprising: a. a first major side, an opposed second major side, a first minor side, an opposed second minor side, a first end and an opposed second end; b. wherein the first major side has a centrally disposed concave area separated from each of the opposed first and second ends by a flattened region; and c. wherein the concave area has a plurality of dimples.
Abstract:
A detergent bar comprising: a. a first major side, an opposed second major side, a first minor side, an opposed second minor side, a first end and an opposed second end; b. wherein the first major side has a centrally disposed concave area separated from each of the opposed first and second ends by a flattened region; and c. wherein the concave area has a plurality of dimples.
Abstract:
Disclosed herein is a process for recovery of pyridine and/or its derivatives from their aqueous mass and/ or manufacturing reaction mass by liquid-liquid extraction employing an environmentally non-hazardous organic solvent. The process further comprising effective recovering and recycle of solvents from the aqueous phase and the other waste obtained during the process.
Abstract:
An oscillator amplifier circuit is provided. The amplifier circuit can be used with a resonator to amplify and form a resonating oscillator. The amplifier circuit comprises an active circuit which includes an inverter and a current-controlled biasing circuit. One transistor of the inverter receives a voltage produced from the biasing circuit in order to place a gate terminal of that transistor at approximately a threshold voltage. The other transistor can be biased using a passive circuit element, such as a resistor. Therefore, both transistors are biased independent of each other within the optimal gain region. Large shunt capacitors are not required and the total current consumption is controlled through a variable resistor coupled to the source terminal of either the first transistor, second transistor, or possibly both transistors of the inverter to adjust the amplitude of the oscillating output.