General MedicationsOPHTHALMICGeneric
LACRISERT
HYDROXYPROPYL CELLULOSE
Standard Dose
5MG
Max Dose
Refer to approved labeling
Primary Use
Review priority: N/A Marketing status: Discontinued
Summary
Approval overview LACRISERT is listed in Drugs@FDA under application 018771 (NDA).
Review priority: N/A Marketing status: Discontinued Active ingredient HYDROXYPROPYL CELLULOSE Form and strength INSERT;OPHTHALMIC - 5MG Sponsor BAUSCH AND LOMB INC Submission history Latest submission status date: 2008-10-30 00:00:00.
Structured Monograph
Clinical summary
Approval overview LACRISERT is listed in Drugs@FDA under application 018771 (NDA). Review priority: N/A Marketing status: Discontinued Active ingredient HYDROXYPROPYL CELLULOSE Form and strength INSERT;OPHTHALMIC - 5MG Sponsor BAUSCH AND LOMB INC Submission history Latest submission status date: 2008-10-30 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Discontinued
- • Review priority: N/A
Interaction Notes
- No interaction notes stored yet.