Packaging and storage
Preserve in tight containers.
Labeling
Label Oral Solution to state both the content of theophylline sodium glycinate and the content of anhydrous theophylline.
Identification
Mix a volume of Oral Solution, equivalent to about 500 mg of theophylline, with 10 mL of 6 N ammonium hydroxide, and evaporate on a steam bath to a volume of about 20 mL. Neutralize with 6 N acetic acid to litmus, and cool, with stirring, to about 15
. Collect the precipitate on a filter, wash with cold water, and dry at 105
for 4 hours: the theophylline so obtained melts between 270
and 274
, the procedure for
Class I being used (see
Melting Range or Temperature 741), and meets the requirements for
Identification test
B under
Theophylline Sodium Glycinate.
Assay
Buffer solution, Mobile phase, Internal standard solution, Standard preparation, and Chromatographic system
Prepare as directed in the
Assay under
Theophylline.
Assay preparation
Transfer an accurately measured volume of Oral Solution, equivalent to about 220 mg of theophylline sodium glycinate, to a 100-mL volumetric flask, dilute with water to volume, and mix. Transfer 10.0 mL of this solution to a 100-mL volumetric flask, add 20.0 mL of Internal standard solution, dilute with Mobile phase to volume, and mix.
Procedure
Proceed as directed for
Procedure in the
Assay under
Theophylline. Calculate the quantity, in mg, of anhydrous theophylline (C
7H
8N
4O
2) in each mL of the Oral Solution taken by the formula:
(1000C/V)(RU / RS),
in which
V is the volume, in mL, of Oral Solution taken, and the other terms are as defined therein.
Auxiliary Information
Staff Liaison :
Daniel K. Bempong, Ph.D., Scientist
Expert Committee : (MDPS05) Monograph Development-Pulmonary and Steroids
USP29NF24 Page 2119
Pharmacopeial Forum : Volume No. 28(2) Page 378
Phone Number : 1-301-816-8143