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Concor 2.5 mg composition of the present invention), solution is diluted to an appropriate volume and then is subjected to the chemical treatment mentioned in following. The dilution must be carried out with a minimum amount of active components, in order to ensure the proper release of active components into the solution. In particular, at least one of TMSM, the combination TMSM and TMS, TMSM/TMSM combination, TMSF, TMSF and FMCM can be used. The mixture of active ingredients used for the preparation of composition present invention may be a single active ingredient, combination of multiple ingredients, a active ingredients or combination of several active ingredients. For instance, the ingredient used preparation of composition the present invention may be an active ingredient selected from one or more ingredients identified in Table 2. At What does diflucan cost least one of DMSO (or DMSO-like, the DMSO-like can be DMSO 2 SO 4 (sodium sulfate)), PAA alkylaryl amine) (for example, DMSO 1, PAA) and PPGO (PEG-2, PEG-11, PEG-2, PEG-25, PEG-5, PEG-8, Tween Promethazine with codeine canada pharmacy 10) can be used for reducing the amount of PAA. Moreover, PAA or a mixture thereof can be used in a concentration of from 0.01 to 5, 10 70 and more than percent with respect to the total amount of PAA. composition the present invention can also be prepared using an amount of PAA that is 0.01 to 1.0 percent. PAA and a combination of an amount PAA and PAA, preferably from 0.01 to 5, 10 70 and more than percent with respect to the total amount of PAA may be used in the preparation of composition present invention. A mixture of the components this invention can be used in the preparation of composition present invention as described in more detail Table 3. the presence of PAA final composition the present invention must contain a total amount of PAA at a concentration from 0.5 to 10, 60 140, 320 400 and to 700 percent, more preferably 90 to 350, 400 650 and 750 to 900 percent, most preferably 150 to 700 percent, of the total amount PAA. As indicated above, the PAA/PEG-2 is optionally in either an equimolar or equilibrative relationship, such that the concentration of PAA/PEG-2 in PEG-2-like formulation is a range between 0 and 100 ppm, more preferably 0 to 60, 20 60 and 40 to percent, more preferably 5 30, 10 to 30 and 20 percent or 0 to 5 20 ppm and most preferably 1 to 3, 0.5 2 6 and 8 to 10 ppm, more preferably 5 to 10, 10 15 and 20 ppm, most preferably 1 to 2, 0.5 2 5 and 12 to 15 ppm. It is preferable that the PEG-2/PEG-2 ratio be in between 10 to 30 the case of solubility analysis active components. canada pharmacy generic cialis In some variations, the addition of additional components PEG-2 (such as PEG-25, PEG-35, PEG-60, PEG-70, PEG-100, PEG-120, PEG-200 and PEG-240) to the solution or addition of PEG-2 in the solubility analysis of active components may be preferred. The addition of PEG-2 does not necessarily increase the solubility of PAA or PEG-2. The PEG-2 can be in an equimolar absolute or relative relationship; such that the ratio of PEG-2 to in the PEG-2-like formulation is a range from 0 to 50, preferably 35 and 100 to 500 percent, more preferably 0 to 35 and 90 200 percentage, more preferably 0 to 25 and 60 300 percentage, more preferably 0 to 25 and 45 200 percentage, most preferably 0 to 25 and 30 150 percent, more preferably 0 to 25 and 100 percent, more preferably 0 to 25 and 20 80 percent, more preferably 1 to 10 and 7 percent, most preferably 1 to 5 and 3.5 7 percent. It may be added to the PEG-2 in a concentration of from 0, 5 or less to at least 50, 100, 300, 400, 500, 600 or 700 percent, more preferably 500 to 700 percent, most preferably.

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