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Tramadol hydrochloride tablet, USP is a centrally acting analgesic. The chemical name for tramadol hydrochloride, USP is (±)cis-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)
cyclohexanol hydrochloride. Its structural formula is:

Molecular formula is C16H13NO2•HCl

The molecular weight of tramadol hydrochloride, USP is 299.8. Tramadol hydrochloride, USP is a white, bitter, crystalline and odorless powder.
It is readily soluble in water and ethanol and has a pKa of 9.41. The n-octanol/water log partition coefficient (logP) is 1.35 at pH7. Tramadol hydrochloride tablets,
USP for oral administration contain 50 mg of tramadol hydrochloride, USP. In addition, each tablet contains the following inactive ingredients: pregelatinized starch,
lactose anhydrous, magnesium stearate, microcrystalline cellulose, polyethylene glycol, sodium starch glycolate, titanium dioxide.

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where to buy tramadol hydrochloride. A total of 455 elderly (65 years of age or older) subjects were expose to tramadol hydrochloride tablets in control clinical trials.
Of those, 145 subjects were 75 years of age and older.

In studies including geriatric patients, treatment-limiting adverse events were higher in subjects over 75 years of age compare to those under 65 years of age.
Specifically, 30% of those over 75 years of age had gastrointestinal treatment-limiting adverse events compare to 17% of those under 65 years of age.
Constipation result in discontinuation of treatment in 10% of those over 75.