Package 71205-193-90

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 71205-193-90
Digits Only 7120519390
Product NDC 71205-193
Product ID 71205-193_e3bdc297-e10a-4632-bf0b-5214ffb84e38
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-193-90)

Marketing

Marketing Status
Marketed Since 2019-01-01
Brand escitalopram
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e3bdc297-e10a-4632-bf0b-5214ffb84e38", "openfda": {"upc": ["0371205193300"], "unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["52df055d-b1c8-4de2-8545-ef08b5bf9c39"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-193-30)", "package_ndc": "71205-193-30", "marketing_start_date": "20190101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-193-60)", "package_ndc": "71205-193-60", "marketing_start_date": "20190101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-193-90)", "package_ndc": "71205-193-90", "marketing_start_date": "20190101"}], "brand_name": "Escitalopram", "product_id": "71205-193_e3bdc297-e10a-4632-bf0b-5214ffb84e38", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71205-193", "generic_name": "Escitalopram Oxalate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}