General MedicationsOPHTHALMICGeneric
PROFENAL
SUPROFEN
Standard Dose
1%
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Discontinued
Summary
Approval overview PROFENAL is listed in Drugs@FDA under application 019387 (NDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient SUPROFEN Form and strength SOLUTION/DROPS;OPHTHALMIC - 1% Sponsor ALCON Submission history Latest submission status date: 2000-02-18 00:00:00.
Structured Monograph
Clinical summary
Approval overview PROFENAL is listed in Drugs@FDA under application 019387 (NDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient SUPROFEN Form and strength SOLUTION/DROPS;OPHTHALMIC - 1% Sponsor ALCON Submission history Latest submission status date: 2000-02-18 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.