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Tetracycline Hydrochloride and Nystatin Capsules
» Tetracycline Hydrochloride and Nystatin Capsules contain not less than 90.0 percent and not more than 125.0 percent of the labeled amount of tetracycline hydrochloride (C22H24N2O8·HCl), and not less than 90.0 percent and not more than 135.0 percent of the labeled amount of USP Nystatin Units.
Packaging and storage
Preserve in tight, light-resistant containers.
Identification
Shake a suitable quantity of Capsule contents with methanol to obtain a solution containing about 1 mg of tetracycline hydrochloride per mL, and filter. Using the filtrate as the Test Solution, proceed as directed under IdentificationTetracyclines
Dissolution
Medium:
water; 900 mL.
Apparatus 2:
75 rpm.
Time:
60 minutes.
Procedure
Determine the amount of tetracycline hydrochloride (C22H24N2O8·HCl) dissolved from UV absorbances at the wavelength of maximum absorbance at about 276 nm of filtered portions of the solution under test, suitably diluted with Dissolution Medium, if necessary, in comparison with a Standard solution having a known concentration of USP Tetracycline Hydrochloride RS in the same Medium.
Tolerances
Not less than 70% (Q) of the labeled amount of C22H24N2O8·HCl is dissolved in 60 minutes.
Loss on drying
Limit of 4-epianhydrotetracycline
Assay for tetracycline hydrochloride
Proceed with Capsules as directed in the Assay under Tetracycline Hydrochloride Capsules.
Assay for nystatin
Proceed as directed for Nystatin under AntibioticsMicrobial Assays
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 4818
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