Package 50090-7177-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 50090-7177-0
Digits Only 5009071770
Product NDC 50090-7177
Product ID 50090-7177_bff6c207-0f4b-42da-8aa1-d8fdd0e55188
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7177-0)

Marketing

Marketing Status
Marketed Since 2024-05-30
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": "bff6c207-0f4b-42da-8aa1-d8fdd0e55188", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["3965ca55-a5ff-4ed0-940c-363d74683fab"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7177-0)", "package_ndc": "50090-7177-0", "marketing_start_date": "20240530"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7177-1)", "package_ndc": "50090-7177-1", "marketing_start_date": "20240530"}], "brand_name": "escitalopram", "product_id": "50090-7177_bff6c207-0f4b-42da-8aa1-d8fdd0e55188", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-7177", "generic_name": "escitalopram", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA078777", "marketing_category": "ANDA", "marketing_start_date": "20230610", "listing_expiration_date": "20261231"}