Active Ingredient: HYDROXYPROPYL CELLULOSE
Proprietary Name: LACRISERT
Dosage Form; Route of Administration: INSERT; OPHTHALMIC
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N018771
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information
