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  2. Levobunolol - Wikipedia

    en.wikipedia.org/wiki/Levobunolol

    Levobunolol is the pure L-enantiomer of bunolol and has more than 60 times the pharmacological activity of D-bunolol. [3] It is used as the hydrochloride, which melts at 209 to 211 °C (408 to 412 °F) and is soluble in water and methanol and slightly soluble in ethanol. [2]

  3. Levobetaxolol - Wikipedia

    en.wikipedia.org/wiki/Levobetaxolol

    It is marketed as a 0.25 or 0.5% ophthalmic solution of levobetaxolol hydrochloride under the trade name Betaxon. Levobetaxolol is a beta-adrenergic receptor inhibitor ( beta blocker ). Indications

  4. Betaxolol - Wikipedia

    en.wikipedia.org/wiki/Betaxolol

    Betaxolol is most commonly ingested orally alone or with other medications for the management of essential hypertension. [4] It is a cardioselective beta blocker, targeting beta-1 adrenergic receptors found in the cardiac muscle.

  5. Dipivefrine - Wikipedia

    en.wikipedia.org/wiki/Dipivefrine

    Dipivefrine, or dipivefrin, also known as epinephrine pivalate and sold under the brand name Propine among others, is a sympathomimetic medication which is used in the treatment of open-angle glaucoma.

  6. Bevantolol - Wikipedia

    en.wikipedia.org/wiki/Bevantolol

    Bevantolol was a drug candidate for angina and hypertension that acted as both a beta blocker and a calcium channel blocker. [1] [2] It was discovered and developed by Warner-Lambert [3] but in January 1989 the company announced that it had withdrawn the New Drug Application; the company's chairman said: "Who needs the 30th beta blocker?"

  7. Acebutolol - Wikipedia

    en.wikipedia.org/wiki/Acebutolol

    Acebutolol is well absorbed from the GI tract, but undergoes substantial first-pass-metabolization, leading to a bioavailability of only 35% to 50%. Peak plasma levels of acebutolol are reached within 2 to 2.5 hours after oral dosing. Peak levels of the main active metabolite, diacetolol, are reached after 4 hours.

  8. Lercanidipine - Wikipedia

    en.wikipedia.org/wiki/Lercanidipine

    Lercanidipine is used in form of the hydrochloride, [4] which is a slightly yellow crystalline powder and melts at 197 to 201 °C (387 to 394 °F) in crystal form I or 207 to 211 °C (405 to 412 °F) in crystal form II. [10] It is readily soluble in chloroform and methanol, but practically insoluble in water. [11]

  9. Etifoxine - Wikipedia

    en.wikipedia.org/wiki/Etifoxine

    The usual dosage of etifoxine (as the hydrochloride salt) is 150 to 200 mg per day in divided doses of 50 to 100 mg two to three times per day (e.g., 50 mg–50 mg–100 mg). [ 2 ] [ 7 ] [ 6 ] [ 18 ] [ 1 ] [ 19 ] [ 20 ] It is taken for a few days to a few weeks, but no longer than 12 weeks.