Package 55700-818-90

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 55700-818-90
Digits Only 5570081890
Product NDC 55700-818
Product ID 55700-818_912b9c5c-2eea-4dd4-a616-57cf796fab62
Description

90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90)

Marketing

Marketing Status
Discontinued 2026-07-20
Brand escitalopram
Generic escitalopram
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": "912b9c5c-2eea-4dd4-a616-57cf796fab62", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["34d14a62-3bdd-405c-82e6-a03302b29860"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55700-818-30)", "package_ndc": "55700-818-30", "marketing_end_date": "20260717", "marketing_start_date": "20191114"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (55700-818-90)", "package_ndc": "55700-818-90", "marketing_end_date": "20260720", "marketing_start_date": "20191114"}], "brand_name": "Escitalopram", "product_id": "55700-818_912b9c5c-2eea-4dd4-a616-57cf796fab62", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55700-818", "generic_name": "Escitalopram", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078032", "marketing_category": "ANDA", "marketing_end_date": "20260720", "marketing_start_date": "20191114"}