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Penicillin G Sodium
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3,3-dimethyl-7-oxo-6-[(phenylacetyl)amino-], 2S-(2 Monosodium (2S,5R,6R)-3,3-dimethyl-7-oxo-6-(2-phenylacetamido)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate » Penicillin G Sodium has a potency of not less than 1500 Penicillin G Units and not more than 1750 Penicillin G Units per mg.
Packaging and storage
Preserve in tight containers.
Labeling
Where it is intended for use in preparing injectable dosage forms, the label states that it is sterile or must be subjected to further processing during the preparation of injectable dosage forms.
USP Reference standards
USP Endotoxin RS. USP Penicillin G Potassium RS. USP Penicillin G Sodium RS.
Crystallinity
pH
Loss on drying
Other requirements
Where the label states that Penicillin G Sodium is sterile, it meets the requirements for Sterility and Bacterial endotoxins under Penicillin G Sodium for Injection. Where the label states that Penicillin G Sodium must be subjected to further processing during the preparation of injectable dosage forms, it meets the requirements for Bacterial endotoxins under Penicillin G Sodium for Injection.
Assay
Mobile phase, Resolution solution, Standard preparation, and Chromatographic system
Proceed as directed in the Assay under Penicillin G Potassium.
Assay preparation
Transfer about 5 mg of Penicillin G Sodium, accurately weighed, to a 50-mL volumetric flask, add about 45 mL of water, and shake to dissolve. Dilute with water to volume, and mix.
Procedure
Proceed as directed in the Assay under Penicillin G Potassium. Calculate the potency, in Penicillin G Units per mg, of Penicillin G Sodium taken by the formula:
(PWS / WU)(rU / rS)
in which WU is the weight of Penicillin G Sodium taken to prepare the Assay preparation, and the other terms are as defined therein.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 3238
Pharmacopeial Forum: Volume No. 27(1) Page 1814
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