Active Ingredient: ESCITALOPRAM OXALATE
Proprietary Name: LEXAPRO
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 5MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021365
Product Number: 001
Approval Date: Nov 27, 2002
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Discontinued
Patent and Exclusivity Information