Abstract: Device for spraying a pulverulent lubricant or release agent dispersed in an air stream onto the pressing tools in a tableting press, having at least one spray nozzle for applying the powder-containing air stream to the pressing tools, a suction system for sucking the excess residues of lubricant off the pressing tools and an air-jet injector for reproducibly loading the air stream with lubricant, wherein the pressing tools are connected to a sensor, which generates an output signal characteristic of the extent to which the lubricant is covering the surfaces of the pressing tools and controls the amount of air sucked off at the suction system, the loading of the air stream with the powder, or both.

Abstract: The invention relates to new combinations of dihydropyridines of the general formula (I) ##STR1## in which R.sup.1 to R.sup.5 have the meaning indicated in the description, for the prevention and treatment of vascular disorders, in particular of cardiovascular and cerebrovascular disorders, containing dihydropyridines having calcium antagonist activity, acetylsalicylic acid nitroesters and vitamins, and, if appropriate, also further auxiliaries or active compounds.

Abstract: The invention relates to pharmaceutical preparations having controlled release of active compound and to processes for their preparation, in particular for poorly soluble active compounds having problematic bioavailability.

Abstract: The invention relates to new derivatives of acetylsalicylic acid (called ASA in the following), which contain an NO.sub.3 structure. They are therapeutically active either as the intact active compound molecule or after cleavage (NO release). The invention also relates to processes for their preparation and their use as medicaments, in particular for the alleviation of pain, inhibition of platelet aggregation, lowering of fever and for the prevention of cardiovascular disorders and oncoses.

Abstract: The present invention relates to the use of cyclic depsipeptides having 18 ring atoms of the general formula (I) ##STR1## in which R.sup.1 to R.sup.6 have the meaning given in the description, and to their optical isomers and racemates, in medicine and veterinary medicine for combating endoparasites, to their preparation, and to new cyclic depsipeptides having 18 ring atoms.

Abstract: The invention relates to the combined use of ketoprofen and specific inorganic basic substances with an improved quality of action.

Abstract: The present invention relates to a ketoprofen liposome gel and a process for its preparation which is distinguished by a simple method of preparation by spontaneous formation of liposomes from phospholipids and ketoprofen.

Abstract: The invention relates to a special process for the preparation of stable, solid medicament formulations of high bioavailability and with controlled release comprising sparingly soluble active compounds and polymeric auxiliaries, and to the formulations thus prepared.

Abstract: The invention relates to stable liposomal injectable formulations for lipophilic, poorly soluble active compounds, in the form of liposomes which are stabilized by short-chain fatty acids, in particular for active compounds from the dihydropyridines group.

Abstract: A method of suppressing ranking fights during assembly of groups of pigs which comprises administering to such pigs an amount effective therefor of a 2-pyrimidinyl-1-piperazine derivative of the formula (I) ##STR1## in which R.sup.1 and R.sup.2 each independently represents at least one radical selected from the groups consisting of hydrogen, C.sub.1-4 -alkyl, halogen, hydroxyl, nitro, C.sub.2-4 -alkenyl, C.sub.1-4 -alkoxy, C.sub.1-4 -alkylthio, C.sub.1-4 -halogenoalkyl, C.sub.1-4 -halogenoalkoxy and C.sub.1-4 -halogenoalkylmercapto,X is a direct bond or a radical N-R.sup.3,R.sup.3 is hydrogen or C.sub.1-4 -alkyl, andA is an optionally substituted alkylene radical with up to 6 C atoms,or a physiologically acceptable salt thereof.