Chlortetracycline Hydrochloride Tablets
» Chlortetracycline Hydrochloride Tablets contain not less than 90.0 percent and not more than 120.0 percent of the labeled amount of C22H23ClN2O8·HCl.
Packaging and storage Preserve in tight containers, protected from light.
Labeling Label the Tablets to indicate that they are intended for veterinary use only.
USP Reference standards 11
USP Chlortetracycline Hydrochloride RS.
USP Oxytetracycline RS.
USP Tetracycline Hydrochloride RS.
Identification Shake a suitable quantity of finely ground Tablet powder with methanol to obtain a solution containing about 0.5 mg of chlortetracycline hydrochloride per mL, and filter. Using the filtrate so obtained as the Test solution, and a methanol solution containing in each mL 0.5 mg of USP Chlortetracycline Hydrochloride RS, 0.5 mg of USP Oxytetracycline RS, and 0.5 mg of USP Tetracycline Hydrochloride RS as the Resolution solution, proceed as directed for Method II under IdentificationTetracyclines 193.
Disintegration 701: 1 hour, simulated gastric fluid TS being used as the test medium in place of water.
Uniformity of dosage units 905: meet the requirements for Weight Variation.
Water, Method I 921: not more than 3.0%, or where the Tablets have a diameter of greater than 15 mm, not more than 6.0%, a quantity of finely ground Tablet powder, accurately weighed, being used.
Assay Transfer not less than 5 Tablets to a high-speed glass blender jar containing an accurately measured volume of 0.01 N hydrochloric acid, so that after blending for 3 to 5 minutes a solution of convenient concentration is obtained. Proceed as directed for chlortetracycline under AntibioticsMicrobial Assays 81, using an accurately measured volume of this solution diluted quantitatively and stepwise with water to obtain a Test Dilution having a concentration assumed to be equal to the median dose level of the Standard.
Auxiliary Information Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 1920