Package 65162-705-88

Brand: escitalopram oxalate

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 65162-705-88
Digits Only 6516270588
Product NDC 65162-705
Product ID 65162-705_d29f980a-e696-4020-8bf9-8f81016c0699
Description

240 mL in 1 BOTTLE (65162-705-88)

Marketing

Marketing Status
Marketed Since 2011-09-03
Brand escitalopram oxalate
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d29f980a-e696-4020-8bf9-8f81016c0699", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["09894a38-4e3a-475d-96cd-c6c8ed87869a"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (65162-705-88)", "package_ndc": "65162-705-88", "marketing_start_date": "20110903"}], "brand_name": "Escitalopram Oxalate", "product_id": "65162-705_d29f980a-e696-4020-8bf9-8f81016c0699", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65162-705", "generic_name": "Escitalopram", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA202227", "marketing_category": "ANDA", "marketing_start_date": "20110903", "listing_expiration_date": "20261231"}