General MedicationsOPHTHALMICGeneric
FML-S
FLUOROMETHOLONE; SULFACETAMIDE SODIUM
Standard Dose
0.1%;10%
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview FML-S is listed in Drugs@FDA under application 019525 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient FLUOROMETHOLONE; SULFACETAMIDE SODIUM Form and strength SUSPENSION/DROPS;OPHTHALMIC - 0.1%;10% Sponsor ALLERGAN Submission history Latest submission status date: 2005-03-10 00:00:00.
Structured Monograph
Clinical summary
Approval overview FML-S is listed in Drugs@FDA under application 019525 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FLUOROMETHOLONE; SULFACETAMIDE SODIUM Form and strength SUSPENSION/DROPS;OPHTHALMIC - 0.1%;10% Sponsor ALLERGAN Submission history Latest submission status date: 2005-03-10 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.