SANDOZ
Sandoz is an international pharmaceutical company specializing in the production of biosimilars and generics (generic medicines containing an active pharmaceutical ingredient identical to that previously invented and patented by another company) for the treatment of infectious diseases, dermatological diseases, respiratory diseases, diseases of the cardiovascular system and the central nervous system , ophthalmic and anesthetic drugs, drugs for the treatment of rheumatological and oncological diseases, hormonal therapy.
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Features:A herbal medicine used to relieve sleep disorders (such as sleeplessness and difficulty falling asleep) and mild states of nervous tension (e.g. fatigue, nervousness and irritability).Recommended daily intake:Mild nervous tension: 1 tablet up to 3 times a daySleep disturbance: 1 tablet in h..
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Pharmacological propertiesPharmacodynamics. Ramiprilat, the active metabolite of ramipril, inhibits the enzyme dipeptidylcarboxypeptidase i (synonyms: apf, kininase ii). in blood plasma and tissues, this enzyme catalyzes the conversion of angiotensin i into the active vasoconstrictor substance angio..
In Stock
Pharmacological propertiesPharmacodynamics. Ramiprilat, the active metabolite of ramipril, inhibits the enzyme dipeptidylcarboxypeptidase i (synonyms: apf, kininase ii). in blood plasma and tissues, this enzyme catalyzes the conversion of angiotensin i into the active vasoconstrictor substance angio..
In Stock
Pharmacological propertiesPharmacodynamics. Ramiprilat, the active metabolite of ramipril, inhibits the enzyme dipeptidylcarboxypeptidase i (synonyms: apf, kininase ii). in blood plasma and tissues, this enzyme catalyzes the conversion of angiotensin i into the active vasoconstrictor substance angio..
5-10 Days
Pharmacological propertiesBudesonide is a synthetic GCS with a pronounced anti-inflammatory and antiallergic effect. when used in therapeutic doses, it almost does not resorb. does not show mineralocorticoid activity, is well tolerated with prolonged treatment.The preparation inhibits the release of..
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