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Tazobactam Sodium
C10H11N4NaO5S 322.27
4-Thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid, 3-methyl-7-oxo-3-(1H-1,2,3-triazol-1-ylmethyl)-, 4,4-dioxide, sodium salt, [2S-(2α,3β,5α)]-;
Sodium (2S,3S,5R)-3-methyl-7-oxo-3-(1H-1,2,3-triazol-1-ylmethyl)-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4,4-dioxide [89785-84-2]

BRIEFING

Tazobactam Sodium. Because there is no existing USP monograph for this drug substance, a new monograph based on validated methods of analysis is proposed.

  1. The liquid chromatographic procedure used in the Assay is based on validation performed using the Inertsil ODS-3 C18 brand of column with L1 packing. The typical retention time for tazobactam is about 7 min.

  2. The liquid chromatographic procedure used in the Organic Impurities test is based on validation performed using the XBridge C18 brand of column with L1 packing. The typical retention time for tazobactam is about 12 min.

Description and Solubility information: White or off-white powder. Very soluble in water; soluble in alcohol; insoluble in ethyl acetate.

 (SM1: P. Pabba, C. Hiemer)

 Correspondence Number—C132775

USP REFERENCE STANDARDS FOR PURCHASE

USP Tazobactam RS
USP Tazobactam Related Compound A RS
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