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Table 5 Results of stability of solution

From: Development and validation of a stability-indicating RP-HPLC method for estimation of Lefamulin in pure and pharmaceutical drug products

Time intervals

% Recoverya

Tablet sample solution (%)

Injection sample solution (%)

Initial

101.21

99.68

After 6 h

100.59

100.12

After 12 h

101.25

99.29

After 24 h

100.11

99.21

After 36 h

99.89

98.49

After 48 h

99.31

97.89

  1. aMean of three measurements