General MedicationsORALGeneric
TRICLOS
TRICLOFOS SODIUM
Standard Dose
750MG
Max Dose
Refer to approved labeling
Primary Use
Marketing status: Discontinued
Summary
Approval overview TRICLOS is listed in Drugs@FDA under application 016809 (NDA).
Marketing status: Discontinued Active ingredient TRICLOFOS SODIUM Form and strength TABLET;ORAL - 750MG Sponsor SANOFI AVENTIS US Submission history See approval history documents.
Structured Monograph
Clinical summary
Approval overview TRICLOS is listed in Drugs@FDA under application 016809 (NDA). Marketing status: Discontinued Active ingredient TRICLOFOS SODIUM Form and strength TABLET;ORAL - 750MG Sponsor SANOFI AVENTIS US Submission history See approval history documents.
Monitoring
- • Marketing status: Discontinued
Interaction Notes
- No interaction notes stored yet.