Clindamycin Palmitate Hydrochloride for Oral Solution
» Clindamycin Palmitate Hydrochloride for Oral Solution is a dry mixture of Clindamycin Palmitate Hydrochloride and one or more suitable buffers, colors, diluents, flavors, and preservatives. It contains the equivalent of not less than 90.0 percent and not more than 120.0 percent of the labeled amount of clindamycin (C18H33ClN2O5S), the labeled amount being 15 mg per mL when constituted as directed in the labeling.
Packaging and storage
Preserve in tight containers.
Uniformity of dosage units 905
For Solid Packaged in Single-unit Containers:
meets the requirements.
Deliverable volume 698:
meets the requirements.
pH 791:
between 2.5 and 5.0, in the solution constituted as directed in the labeling.
Water, Method I 921:
not more than 3.0%.
Assay
Internal standard solution
and Standard preparationPrepare as directed in the Assay under Clindamycin Palmitate Hydrochloride.
Assay preparation
Constitute the Clindamycin Palmitate Hydrochloride for Oral Solution as directed in the labeling, and transfer 5.0 mL of the constituted solution to a glass-stoppered, 15-mL conical centrifuge tube. Add 5.0 mL of Internal standard solution and 1 mL of sodium carbonate solution (3 in 10), and proceed as directed for Standard preparation, in the Assay under Clindamycin Palmitate Hydrochloride, beginning with Insert the stopper, shake vigorously.
Procedure
Proceed as directed in the Assay under Clindamycin Palmitate Hydrochloride. Calculate the quantity, in mg, of C18H33ClN2O5S in each mL of the solution constituted from Clindamycin Palmitate Hydrochloride for Oral Solution taken by the formula:
(F / 1000)(WS / V)(RU / RS)
in which V is the volume, in mL, of constituted solution from Clindamycin Palmitate Hydrochloride for Oral Solution taken, and the other terms are as defined therein.
Auxiliary Information
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Chromatographic Column
USP32NF27 Page 1969
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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