Package 72162-2242-0

Brand: escitalopram oxalate

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 72162-2242-0
Digits Only 7216222420
Product NDC 72162-2242
Description

1000 TABLET in 1 BOTTLE (72162-2242-0)

Marketing

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

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a3f1acbc-6b69-4ce6-95a7-e51a2023ea50", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351249"], "spl_set_id": ["a0ff752d-cb30-4131-a7d6-cd66d8a47b1a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2242-0)", "package_ndc": "72162-2242-0", "marketing_start_date": "20120911"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2242-1)", "package_ndc": "72162-2242-1", "marketing_start_date": "20120911"}], "brand_name": "escitalopram oxalate", "product_id": "72162-2242_a3f1acbc-6b69-4ce6-95a7-e51a2023ea50", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "72162-2242", "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": "5 mg/1"}], "application_number": "ANDA090939", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}