Package 50090-6897-0

Brand: escitalopram

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 50090-6897-0
Digits Only 5009068970
Product NDC 50090-6897
Product ID 50090-6897_8c40f650-b61d-47e9-9053-e6653541d516
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6897-0)

Marketing

Marketing Status
Marketed Since 2023-12-11
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": "8c40f650-b61d-47e9-9053-e6653541d516", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["575d7755-0518-4d48-bb1a-4ad01321fde7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6897-0)", "package_ndc": "50090-6897-0", "marketing_start_date": "20231211"}], "brand_name": "Escitalopram", "product_id": "50090-6897_8c40f650-b61d-47e9-9053-e6653541d516", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50090-6897", "generic_name": "Escitalopram", "labeler_name": "A-S Medication Solutions", "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_start_date": "20160201", "listing_expiration_date": "20261231"}