Labeling
It meets the requirements for
Labeling under
Injections 1. The label states that it is to be thawed just prior to use, describes conditions for proper storage of the resultant solution, and directs that the solution is not to be refrozen.
Identification
The chromatogram of the
Assay preparation obtained as directed in the
Assay exhibits a major peak for ceftriaxone, the retention time of which corresponds to that exhibited in the chromatogram of the
Standard preparation obtained as directed in the
Assay.
Assay
pH 7.0 Buffer, pH 5.0 Buffer, Mobile phase, Standard preparation, Resolution solution, and Chromatographic system
Prepare as directed in the
Assay under
Ceftriaxone Sodium.
Assay preparation
Allow 1 container of Injection to thaw, and mix. Transfer an accurately measured volume of the Injection, equivalent to about 40 mg of ceftriaxone, to a 200-mL volumetric flask, dilute with Mobile phase to volume, and mix. Use this solution promptly after preparation.
Procedure
Proceed as directed for
Procedure in the
Assay under
Ceftriaxone Sodium. Calculate the quantity, in mg, of ceftriaxone (C
18H
18N
8O
7S
3) in each mL of the Injection taken by the formula:
200(C / V)(rU / rS),
in which
V is the volume, in mL, of Injection taken; and the other terms are as defined therein.