Package 72162-2241-0

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 72162-2241-0
Digits Only 7216222410
Product NDC 72162-2241
Product ID 72162-2241_3bb03754-0437-4f83-8ad5-0970d9788c01
Description

1000 TABLET, FILM COATED in 1 BOTTLE (72162-2241-0)

Marketing

Marketing Status
Marketed Since 2012-09-11
Brand escitalopram oxalate
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3bb03754-0437-4f83-8ad5-0970d9788c01", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332"], "spl_set_id": ["0de88dad-d54c-4773-a5d6-a705e012973a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (72162-2241-0)", "package_ndc": "72162-2241-0", "marketing_start_date": "20120911"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2241-1)", "package_ndc": "72162-2241-1", "marketing_start_date": "20120911"}], "brand_name": "escitalopram oxalate", "product_id": "72162-2241_3bb03754-0437-4f83-8ad5-0970d9788c01", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2241", "generic_name": "escitalopram oxalate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}