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