Примери за използване на Other pharmaceutical forms на Английски и техните преводи на Български
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Ecclesiastic
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Computer
Other pharmaceutical forms may be available for this population.
If a longer duration of use is required, other pharmaceutical forms are available.
Other pharmaceutical forms/strengths may be more appropriate for this population.
For paediatric patients who have difficulties swallowing tablets, other pharmaceutical forms are available.
Other pharmaceutical forms/strengths may be more appropriate for administration.
For older children it may be feasible to substitute tablets for the maintenance dose of other pharmaceutical forms.
Other pharmaceutical forms/strengths may be more appropiriate for this population.
For children under 45 kg other pharmaceutical forms of azithromycin, e.g. suspensions, may be used.
Other pharmaceutical forms/strengths may be more appropriate for administration to this population.
In respect of syrups, emulsions,granular preparations and other pharmaceutical forms to be administered in measured quantities, by the mass or units of biological activity of each active substance per measured quantity.
Other pharmaceutical forms/strengths may be more appropriate for administration to this population.
Other pharmaceutical forms/strengths may be more appropriate for administration to this population.
Other pharmaceutical forms/strengths are available which can be appropriately be dosed for smaller children.
Other pharmaceutical forms/strengths are available which can be appropriately be dosed for smaller children(see section 4.3).
Other pharmaceutical forms/strengths are available which can be appropriately dosed for infants below the age of 3 months.
Other pharmaceutical forms are available for administration to patients≤20 kg and other younger patients who are not able to swallow tablets.
Other pharmaceutical forms are available for administration to patients≤ 20 kg and other younger patients who are not able to swallow tablets.
Lt; Other pharmaceutical forms/strengths may be more appropriate for administration>< This formulation is not suitable for administration>
Other pharmaceutical forms may be more appropriate for administration to patients≤ 20 kg and other younger patients who are not able to swallow tablets.
Lt; Other pharmaceutical forms/strengths may be more appropriate for administration to this/these population(s)>< This formulation is not suitable for administration to this/these population(s)>
Other dosages and pharmaceutical forms are available in Germany only.
The other dosages and pharmaceutical forms are only available in Germany.
For adults and adolescents 15 years and over(>53 kg) other strengths or pharmaceutical forms are available.
But other pharmaceutical companies continued to manufacture it in less pure forms.
Scientific name or other name given in a pharmacopoeia of the homeopathic stock or stocks, together with a statement of the route of administration, pharmaceutical form and degree of dilution to be registered;
Following the granting of a marketing authorisation, the authorisation holder may allow use to be made of the pharmaceutical, preclinical and clinical documentation contained in the file on the medicinal product,with a view to examining subsequent applications relating to other medicinal products possessing the same qualitative and quantitative composition in terms of active substances and the same pharmaceutical form.
For the purpose of harmonisation under this Article similar veterinary medicinal products shall refer to products,not all of which are bioequivalent, and other than homeopathic veterinary medicinal products, that have the same active substance or active substances and the same pharmaceutical form or a range of veterinary medicinal products belonging to the same therapeutic class.
If test procedures and limits other than those mentioned in the relevant monographs and general chapters of the European Pharmacopoeia, or failing this, in the pharmacopoeia of a Member State are used, this shall be justified by providing proof that the finished product would, if tested in accordance with those monographs, meet the quality requirements of that pharmacopoeia for the pharmaceutical form concerned.
Where an initial marketing authorisation has been granted for a medicinal product in accordance with the first subparagraph, all other strengths, pharmaceutical forms, routes of administration and forms of administration, as well as any modifications and extensions referred to in the first subparagraph, shall be approved or included in the initial marketing authorisation.
Following the granting of a marketing authorisation, the authorisation holder may allow use to be made of the pharmaceutical, preclinical and clinical documentation contained in the file on the medicinal product,with a view to examining subsequent applications relating to other medicinal products possessing the same qualitative and quantitative composition in terms of active substances and the same pharmaceutical form.